Oral Electrolyte Solution Pedialyte

Iodine cotton swabs : 1.Povidone-iodine solution 5% 2.100% cotton combed cotton+plastic stick 3. Length : 7.8cm*0.5cm 4. 500pcs/inner box, 12boxes/carton, 6000piece/carton 5.Delivery time: 3-15days after deposited depend on order quantity Applications: For disinfecting skin wounds with clean-up. Minor skin damage, abrasions, cuts, burns and other superficial skin and wound disinfection. Blood, intramuscular, intravenous infusion prior to skin disinfection. Skin sores xian verification, mouth inflammation of the nasal cavity, oral ulcers, vaginal mucous membrane disinfection. Especailly suitable use in hospital and first aid for this bulk package. Warning: for external use only, keep out of eyes, non-sterile, discontinue use if irritation occurs. Don't insert in ear canal. Keep at room temperature. Avoid direct sunlight. 500pcs/inner box, 12boxes/carton, 6000piece/carton

We provide various concentration of electrolyte Sodium (Na+ ) 135-140 Mmol/L Chloride (Cl- ) 110-122 Mmol/L Potassium (K+ ) 0-3 Mmol/L Calcium ( Ca+) 0-2 Mmol/L BICARBONATE ( HCO3- ) 27-39 Mmol/L ACETATE (CH3COO- ) 2-5 Mmol/L Product Descripition Part A Solution available in 4 Litre,5 Litre and and 10 litre. Part B available in powder form for 1 and 5 Dialysis sessions (4 Hours each) it is available in any custom formation Advantages Custom Formulations Pyrogen-free Product Part A is sealed and leak-proof, packed in Pharma-grade HDPE canisters (cans) Part B is in powder form hence saves lot of volume, freight with easy handling Part B is of highest quality (BP/EP) and is granulated for easy flow. Mixing is excellent with no residue Precision in Formulation, hence easy calibrations on dialysis machine

Hot spot: 1. Accuracy meet ASTM Standard 2. Fast testing to get the data within one second 3. Can save 8 sets latest testing data 4. Small size and 70g weight for easy carry 5. Comply with CMDCAS CE0197 ISO9001&13485 FDA and EN46001 certificates. 6. Testing parts are the ear canal without much influence from environment 7. Eco-friendly without any pollution and safe testing 8. Best design and quality control Specification: 1. Temperature range 34 ~42.2 ¡ìo 93.2 H~108 H 2. Environment Temperature range: 5 ~40 ¡ìo 41 H~104 H 3. Temperature solution 0.1 or 0.1 H ¡ìo 4. Accuracy 5. Free Transfer from C to F / H 6. Storage Environment Temperature -25 ~55 ¡ìo -13 H~131 H 7. Maximum Humidity (max): 85%RH, non-condensing 8. Information on the clinical repeatability: 0.15 9. Temperature Model: Close to Oral Temperature 10. Memory: up to 8 sets testing data can be stored 11. Background light LCD screen 12. Power One piece 3V CR2032 Lithium battery 13. Battery Standby 2 years or 4000 times testing 14. Size 101mm 34mm 28mm 15. Weight: Around 70g (including cell). Package: Accessory-20pcs probe cover, user manual, plastic inner box, color outer box 1pc/inner box and with color outer box Inner box size: 11.2*6.6*3.2CM Outer box size: 14.2*9.3*6.0CM 50pcs/carton Carton Size: 47*31*35CM Gross Weight: 10.5KG/Carton.

1.Product Identification Name: Disposable virus sampling tube Packaging Specification: Type (Inactivated) :0.5ml, 1ml, 1.5ml, 2ml, 2.5ml, 3ml, 4ml, 5ml, 10ml; Type â?¡ (Non-inactivated) :0.5ml, 1ml, 1.5ml, 2ml, 2.5ml, 3ml, 4ml, 5ml, 10ml; Type â?¢ (With swabs) : 6cm, 7cm, 7.5cm, 8cm, 8.5cm, 9cm, 10cm, 12cm, 15cm, 17cm, 20cm, 22cm, 25cm Storage and Stabilityï¼? 1.The product should be stored in a dark, dry and cool environment. Avoid prolonged exposure to light. 2.Do not bump during transportation to avoid the sampling tube from rupturing; do not squeeze to avoid deformation of the sampling tube. 3.The product is valid for 12 months. 2.Intended use The disposable virus sampling tube can be used for the collection, transportation and storage of clinical samples. 3.Classification Information and Conformity Assessment Route The product falls into OTHERS in accordance to Directive 98/79/EC of the European parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices. Annex III EC DECLARATION OF CONFORMITY in 98/79/EC Directive is chosen as conformity assessment procedure. 4.Procedure 1.Open the package, take out the single-use virus sampling tube, and mark relevant information; 2.Take the matching swab and place it on the area where the specimen needs to be collected (such as the nasal cavity, oral cavity, throat, vagina, urethra, etc.), and gently wipe it more than 15 times to collect the sample. 3.Open the cover of the sampling tube, insert the swab of the collected sample into the sampling tube and break it from the fragile part, insert the swab head into the preservation solution in time, and tighten the tube cap; 4.Place the tightened virus sampling tube properly, and then transport to the inspection department for inspection within 48 hours.

NeoSAFE is a non-invasive diagnostic device for standardized assessment and monitoring of the newborn oral feeding ability. Feeding maturity is characterized as the coordination of sucking-swallow and respiration. NeoSAFE provides a method to assess this coordination maturity objectively and assesses the feeding ability of newborns by monitoring respiration and swallow activities of infants while utilizing two non-invasive probes attached to the baby during a feeding session. This solution utilizes the state-of-the-art signal processing and machine learning algorithms. So far, NeoSAFE has successfully completed the CE certification process with a clinical safety report (CSR) and two clinical studies. Besides that, NeoSAFE has been funded by EU Horizon 2020 SME Instrument twice in a row

Product Details: Number of Reactions(Preps)/Kit : 1000 Brand ; Thermofisher Test Method : (SARS-CoV-2) RT-PCR Sample Type : Nasal & Oral Swab The Applied Biosystems TaqPath COVID-19 Combo Kit is a fast, highly sensitive multiplex diagnostic solution that contains the assays and controls needed for the real-time PCR detection of RNA from the SARS-CoV-2 virus. Features of the newly developed multiplex diagnostic kit: A complete workflow from viral RNA extraction from up to 94 specimens and genetic analysis using real-time PCR to diagnostic report generation in under 4 hours Targeted specificity to 100% of currently available complete genomes for SARS-CoV-2 Assay targets spike (S) protein and nucleocapsid (N) protein regions having higher specificity and exhibiting lower risk for mutation COVID-19 Interpretive Software, which automatically converts genetic analysis data into diagnosis, helping reduce risk of user interpretation error The TaqPath COVID-19 Combo Kit consists of both the TaqPath RT-PCR COVID-19 Kit and the TaqPath COVID-19 Control Kit for simplified ordering. The kit can be used by clinical and public health laboratories to quickly evaluate up to 94 patient specimens in under 3 hours. The kit is approved for use with RNA extracted from nasopharyngeal swabs, nasopharyngeal aspirate (nasal aspirate), and bronchoalveolar lavage (BAL) from patients at risk of exposure to the SARS-CoV-2 virus or with signs and symptoms of COVID-19 (see product label for Intended Use Statement and product information). The TaqPath COVID-19 Combo Kit is a single, high-throughput (1,000 reactions) kit and is recommended for use with either the Applied Biosystems 7500 Fast Dx Real-Time PCR System or the 7500 Fast Real-Time PCR System (RUO version) and the associated Applied Biosystems COVID-19 Interpretive Software. The TaqPath COVID-19 Combo Kit includes the following components: TaqPath RT-PCR COVID-19 Kit COVID-19 real-time PCR assay multiplexâ??multiplexed assays that contain three primer/probe sets specific to different SARS-CoV-2 genomic regions and primers/probes for bacteriophage MS2 MS2 phage controlâ??internal process control for nucleic acid extraction TaqPath COVID-19 Controlâ??RNA control that contains targets specific to the SARS-CoV-2 genomic regions targeted by the assays TaqPath COVID-19 Control Dilution Buffer dilution buffer for the IVT RNA control as defined in the IFU (information for use)