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"Tengwang" wound treatment kit (unsterilized) - Taiwan Registration 367507f7e02758106357b6297e69acae

Access comprehensive regulatory information for "Tengwang" wound treatment kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 367507f7e02758106357b6297e69acae and manufactured by Tengwang Co., Ltd. The authorized representative in Taiwan is Tengwang Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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367507f7e02758106357b6297e69acae
Registration Details
Taiwan FDA Registration: 367507f7e02758106357b6297e69acae
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Device Details

"Tengwang" wound treatment kit (unsterilized)
TW: "้จฐๆ—บ"ๅ‰ตๅ‚ท่™•็†ๅŒ…(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

367507f7e02758106357b6297e69acae

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of the medical device management measures "external use of non-absorbent gauze or sponge balls (I.4014)", "wound/burn dressings for closure (I.4020)" and "medical adhesive tapes and adhesive bandages (J.5240)".

J General hospital and personal use equipment;; I General, Plastic Surgery and Dermatology

J.5240 Adhesive tapes and adhesive bandages for medical use; I.4020 Wound/burn dressings for closure;; I.4014 Non-absorbent gauze or sponge balls are used externally

Domestic

Dates and Status

Feb 22, 2011

Feb 22, 2016

Apr 25, 2018

Cancellation Information

Logged out

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