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"Tengwang" iodine gauze - Taiwan Registration ba92d1e4c9df982116fa4e18e982af00

Access comprehensive regulatory information for "Tengwang" iodine gauze in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba92d1e4c9df982116fa4e18e982af00 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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ba92d1e4c9df982116fa4e18e982af00
Registration Details
Taiwan FDA Registration: ba92d1e4c9df982116fa4e18e982af00
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Device Details

"Tengwang" iodine gauze
TW: โ€œ้จฐๆ—บโ€็ข˜ๆถฒ็ด—ๅธƒ
Risk Class 2
Cancelled

Registration Details

ba92d1e4c9df982116fa4e18e982af00

DHY00500309001

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.0005 Iodine cotton pad;; I.4014 Non-absorbent gauze or sponge balls are used externally

Domestic

Dates and Status

Sep 07, 2010

Sep 07, 2015

Apr 25, 2018

Cancellation Information

Logged out

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