fda tampons list of supplies 2019

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Ethylene Oxide Sterilization for Medical Devices | FDA- fda tampons list of supplies 2019 ,In May and November 2019, the FDA engaged the infection control community at the ... To report a medical device shortage or supply issue, email Deviceshortagesfda.hhs.gov or phone 1-800-638 ...The Facts on Tampons—and How to Use Them Safely | FDASep 30, 2020·Tampons are medical devices regulated by the U.S. Food and Drug Administration. If you or a loved one uses them, it's important to use them safely. Learn the basics.



CFR - Code of Federal Regulations Title 21 - Food and Drug ...

Oct 01, 2021·CFR - Code of Federal Regulations Title 21. The information on this page is current as of April 1 2020. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). Sec. 801.430 User labeling for menstrual tampons. (a) This section applies to scented or scented deodorized menstrual tampons as ...

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Harm Reduction Supplies - Get Your Drugs Tested

Tampons Cotton Balls Q-Tips . FIRST AID Bandage 1×3 Bandage 2×3 Bandage Finger Bandage Knuckle Gauze 2×2 & 4×4 Gauze Rolls Tensor Bandage Saline . OTHER Syringe Oral 3mL Syringe Oral 10mL . Harm reduction supplies provided by BC Centre for Disease Control. All other items provided by The Medicinal Cannabis Dispensary

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Why are Tampons Classified as Medical Devices? | …

The FDA has developed a guidance document to assist industry in preparing premarket notification submissions (510(k)) for menstrual tampons and pads that are subject to 510(k) requirements. Read more about synthetic fibers in tampons. Tampons and TSS. But the story goes much deeper than just the definition of a medical device.

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Menstrual Tampons and Pads: Information for ... - FDA

1. Introduction. FDA has developed this guidance document to assist industry in preparing premarket notification submissions (510(k)) for menstrual tampons and pads that are subject to 510(k ...

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Guidance for Industry and FDA Staff - Menstrual …

FDA has developed this guidance document to assist industry in preparing premarket notification submissions (510(k)) for menstrual tampons and pads that are subject to 510(k) requirements.

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