Taiwan FDA registration 0dd6c162430f10420c2eec07eaabfe92

"Birch-Lai" external rinse sleeve (sterilized)

TW: “樺萊”外用沖洗套 (滅菌)

Taiwan·Risk Class 1·FAIRY POLYMER INDUSTRY CO., LTD.·Registered Jul 29, 2013 – Jul 29, 2028Active

Registration details

Analysis ID: 0dd6c162430f10420c2eec07eaabfe92

Company information

Manufacturer: FAIRY POLYMER INDUSTRY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FAIRY POLYMER INDUSTRY CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Devices "Introduction/Drainage Catheters and Their Accessories (I.4200)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4200 Incoming/Drainage Tubes and Accessories
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Jul 29, 2013
Expiry Date: Jul 29, 2028

About this record

Access comprehensive regulatory information for "Birch-Lai" external rinse sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0dd6c162430f10420c2eec07eaabfe92 and manufactured by FAIRY POLYMER INDUSTRY CO., LTD.. The authorized representative in Taiwan is FAIRY POLYMER INDUSTRY CO., LTD..

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