Packaging materials, Industrial film & pouch, aluminum foil, KF mask, Alcohol Based Hand Sanitizers, Toilet Safety Handle, Sterilizer for wheelchair/stroller.
Body vibration machine, medical equipment, health care, beauty products, massager, vibrating machine, shower system, shower head.
Odm and oem for cosmetics skincare products such as toner, emulsion, serum, cream, mask pack, pouch, shampoo, conditioner, etc..
It is filled with healthy natural ingredients that have a good effect, such as propolis extract, liquorice extract, sesame extract, and grapefruit seed extract.
- Cement dispenser (PCD system) < component > 1.wire pin 2. Cannular & expander 3. 1st VP needle 4.spacer 5. 3rd cement filler & pusher 6. 2nd cement filler & pusher 7. 1st cement filler & pusher
EXCELLENT PERFORMANCE Maximum efficiency 97.3%, battery efficiency 94.3% Maximum 9kW PV input power Maximum Charge/Discharge current 120A Large MPPT current, compatible with high-power solar panels Advanced parallel function HIGH RELIABILITY Key components from international famous brands IP65 protection rating, good adaptability to complex outdoor environment Multiple protections built-in, optional Type II SPD Natural cooling design INTELLIGENT MAINTENANCE Quick commission through APP, 7*24h remote monitoring, configurating, upgrading Advance energy management mechanism, multiple working modes built-in, Max. Efficiency (PV to AC) 97.30% Max. Efficiency (BAT to AC) 94.30% Euro. Efficiency (PV-AC) 96.80% Input (PV) Max. PV Input Power 6,300W 9,000W Max. PV Voltage SSOV Start-up Voltage 90V MPPT Voltage Range 70V-540V Max. Input Current 15A/15A Max. Short Circuit Current 20A/20A Nos. of MPPT 2 String per MPPT 1-Jan Input/Output (BAT) Battery type Lithium-ion, Lead-acid Nominal Battery Voltage 48V Battery Voltage Range 40V-65V Max. charge/Discharge Current 60A/60A 120A/120A Max. Charge/Discharge Power 3,000W/3,000W 6,000W/6,000W Output (Grid) Nominal AC Output Power 3,600W 5,000W Max. AC Apparent Power 3,960VA 5,500VA Max.AC Output Power (PFâ??1) 39,60W 5,500W Max. AC Output Current 18A 25A Nominal Grid voltage 220V/230V/240V, L+N+PE Grid Voltage Range 150V-300V (Adjustable) Nominal Grid Frequency 50Hz/60Hz Grid Frequency Range 45Hz-55Hz/55Hz-65Hz (Adjustable) Power factor THDI >� � � � � � � � � � � � � � � � � � � � � � � � � � � � � 0.99 @rated power (Adjustable 0.8 LD - 0.8 LG) <3% (Rated Power) Output (Back up) Nominal Output Power 3,000W S,000W Nominal Output Current 13A 21.7A Peak Power(>1 s) 4,500VA 7,500VA Nominal Output Voltage 220V/230V/240V, L+N+PE Nominal Output Frequency 50Hz/60Hz Transfer Time <1Oms THDV <3% @100% R Load Protection Protection Category Class I DC switch Yes Anti-islanding Protection Yes AC Over Current Protection Yes AC Over Voltage Protection Yes AC Short Circuit Protection Yes DC Reverse Protection Yes Surge Arrested DC Type III, AC Type III PV Insulation Detection Yes Leakage Current Protection Yes General Max. Operation Altitude 4000m (>2000m derating) Protection Degree IP65 Operating Temperature Range -25â??C-60 % (>45 % debating) Relative Humidity 0-100% Cooling Natural Cooling Mounting Wall bracket Dimensions (W*H*D) 570mm*495mm*175mm Weight 20Kg 25Kg PV Connection MC4/H4 Battery Connection Dedicated DC connector AC Connection Dedicated AC connector HMI & COM Display LED+APP Communication Interface Certification RS485/CAN (for BMS), RS485, USB, DRM/RS485 (for Meter), Optional: Wi-Fi/GPRS/LAN Grid VDE-AR-N4105, IEC 61727/62116, AS 4777.2, EN 50549-1, C10/11 Warranty 5 years Safety IEC 62109-1&2, IEC 62477-1
Fermented Red Ginseng Extract(The Power of 456 Hours) 80ml Cofilia fermented red ginseng extract is a liquid product made using fermented red ginseng made by patented method. The name of the product means the time when each product is made. It is a product that contains the power of ginseng during the time of fermentation, drying, and extracting fermentation. Fermented red ginseng extract (the power of 456 hours) 80ml shall be dried for 3 days after fermentation of ginseng on 14 days, and shall be extracted for 2 days.
Fermented Black Ginseng Extract(The Power of 648 Hours) 80ml Cofilia fermented black ginseng extract is a liquid product made using fermented black ginseng made by patented method. The name of the product means the time when each product is made. It is a product that contains the power of ginseng during the time of fermentation, drying, and extracting fermentation. Fermented black ginseng extract(the power of 648 hours) 80ml shall be dried for 5 days after fermentation of ginseng on 20 days, and shall be extracted for 2 days
Fermented Black Garlic Extract (The Power of 504 Hours) 80ml: Cofilia fermented black garlic extract is a liquid product made using fermented black garlic made by the patented method. The name of the product means the time when each product is made. It is a product that contains the power of garlic during the time of fermentation, drying, and extracting fermentation. Fermented black garlic extract (the power of 504 hours) 80ml shall be dried for 5 days after fermentation of garlic on 14 days, and shall be extracted for 2 days.
Helicobacter pylori is a parasitic bacterium in the stomach that lives between the gastric mucosa and mucus. According to the WHO, more than half of the world's population has H. pylori and is the third leading cause of cancer-related deaths. In 1994, the WHO's IARC classified H. Pylori as a Class 1 carcinogen. The incidence of H. pylori in developing countries is the highest worldwide, highlighting the need for highly accurate and manageable testing. By 2025, the H. pylori testing market is expected to be worth 6 billion. Accordingly, SML Genetree has developed a reagent that can diagnose Helico-bacter pylori and Clarithromycin-resistant mutants (A2142G, A2143G) through DNA extracted from human hygienic tissue using Real-time Polymerase Chain Reaction. Since it contains multiple gene regions, Helico-bacter pylori and Clarithromycin-resistant mutations can be detected sensitively, and high reproducibility has been demonstrated through repeated tests by serially diluting various positive samples and standards. In addition, as a result of clinical evaluation on human sanitary inspection tissue by commissioning a large domestic consignment inspection institution, high sensitivity and specificity were confirmed, proving its excellent clinical performance.
HPV is a virus that causes papillomas (benign tumors), and about 200 types have been discovered so far. Some types of HPV are known to be the direct cause of cervical cancer, head and neck cancer, etc. In particular, in the case of cervical cancer, more than 99% of the causes are reported to be caused by HPV. If it is detected early, it is easy to treat, but if it is detected late, the 5-year survival rate is less than 15% even with treatment, so regular check-ups are very important. SML Genetree has developed the world's first Ezplex�® HPV NGS Kit to diagnose HPV using the NGS method. Unlike the existing methods that only detected up to 20 to 40 types and only positive-negative, NGS was introduced to provide positive results for 45 types of HPV (up to 100 types including for export) according to the amount of DNA detected in steps 1 to 3 Semi-quantitative inspection of the level is possible. It has a high level of automation that is close to full automatic. The time has been shortened so that up to 480 people can be analyzed within 16 hours with one analysis, and it is possible to distinguish HPV species that were difficult to distinguish precisely. Unlike the existing sequencing method, the NGS method has been highly evaluated for its potential as a precision medical technology that can dramatically reduce time and cost by analyzing numerous DNAs at high speed. As a result of clinical efficacy evaluation with more than 2500 clinical specimens in large domestic hospitals, it is a product with high sensitivity and specificity compared to existing tests.
Ezplex�® SARS-CoV-2 G Kit, developed by SML Genetree, is a product that has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA). This is an in vitro diagnostic test that qualitatively detects the nucleic acids of SARS-CoV-2 (RdRp and N genes) in sputum to aid in emergency screening for COVID-19. This product can be used for a large amount of screening tests because it can perform a pooling test, unlike the products that the existing domestic companies have approved for emergency use by the FDA. For the combined test, samples are collected in units of 5 people and tested. If positive, individual tests are performed. In the case of a negative test, all tests are performed in a negative way. In particular, since a large number of samples are tested at once, the test is only possible with high sensitivity and specificity compared to existing diagnostic kits. According to the FDA, it was confirmed that 100% agreement was achieved in the result comparison test of individual and collective tests, and it was the 20th in the world and the first Korean company to pass the test. Excellent clinical performance was demonstrated by confirming high sensitivity and specificity through clinical evaluation, and stability was confirmed for 12 months through long-term storage tests. In January 2021, it was officially approved by the Korean Ministry of Food and Drug Safety (MFDS).
Ezplex MTBC/NTM Real-time PCR Kit is an in vitro diagnostic test that simultaneously detects Mycobacterium tuberculosis complex (MTBC) and 20 types of nontuberculous mycobacteria (NTM). Sensitivity : Multiple gene targets for MTBC and NTM. Clinical Performance: Validated clinical performance. Fast Results: Testing can be completed within 2 hours post extraction.
Ezplex Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction Comprehensive Panel- One test can identify 19 respiratory viruses and 6 bacterial species simultaneously. Sensitivity Detection of all targeted viruses and bacteria with high sensitivity. Convenience Genetree Viewer analysis software available for users to conveniently produce test results. Clinical Performance: Clinical testing confirmed the high sensitivity and specificity. Stability: Shelf life of up to 12 months. Analytical Specificity: Testing of 31 species of microorganisms showed no cross reactivity.
Ezple Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction.
MTBC/NTM Real-time PCR Kit is an in vitro diagnostic test that simultaneously detects Mycobacterium tuberculosis complex (MTBC) and 20 types of nontuberculous mycobacteria (NTM).
HP-CLA Real-time PCR kit is an in vitro diagnostic test that qualitatively detects helicobacter pylori and Clarithromycin-resistant mutations from human gastric biopsy tissues. Contains multiple gene targets to detect Helicobacter clarismycin-resistant mutations. Genetree Viewer analysis software is provided, allowing users to conveniently check results.
HLA-DRB1 NGS typing Kit is an in vitro diagnostic test that detects and distinguishes allelic genes of HLA-DRB1 in human leukocyte antigens at high resolution using next-generation sequencing. Ezplex's unique amplicon approach simplifies the traditional complex NGS Library construction process and provides dedicated software optimized for HLA typing for easy analysis. The Ezplex�® HLA-DRB1 NGS typing Kit accurately reads the HLA-type Acuracy % (95% Confidence Interval) in DRB1 Locus within a total of 35 hours from DNA extraction to NGS results analysis to help with pre-transplant testing.
STD12 Real-time PCR Kit is an in vitro diagnostic test that simultaneously detects 12 types of pathogens that cause sexually transmitted infections
SFTS Virus Real-time PCR Kit is an in vitro diagnostic test intended for the qualitative detection of the Dabie bandavirus that causes Severe Fever with thrombocytopenia Syndrome using nucleic acid RNA extracted from human blood or serum. Clinical evaluation performed with human blood specimens confirmed clinical accuracy. High reproducibility with similar results were confirmed various tests.
