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"K.F."SURGICAL APPAREL PACK - Taiwan Registration d940fd5c234ae9f08373443481fd87b9

Access comprehensive regulatory information for "K.F."SURGICAL APPAREL PACK in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d940fd5c234ae9f08373443481fd87b9 and manufactured by Guofa Medical Equipment Co., Ltd. The authorized representative in Taiwan is Guofa Medical Equipment 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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d940fd5c234ae9f08373443481fd87b9
Registration Details
Taiwan FDA Registration: d940fd5c234ae9f08373443481fd87b9
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Device Details

"K.F."SURGICAL APPAREL PACK
TW: "ๅœ‹็™ผ"ๆ‰‹่ก“่กฃ็‰ฉๅŒ…
Risk Class 2
MD

Registration Details

d940fd5c234ae9f08373443481fd87b9

Department of Health Medical Device Manufacturing No. 001823

DHY00500182305

Company Information

Taiwan, Province of China

Product Details

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

I General and plastic surgical devices

Produced in Taiwan, China

Dates and Status

May 30, 2006

May 30, 2026