Taiwan FDA registration b906a54b06eccbf61e45a15c5b066f6c
"Gelidine" negative pressure wound treatment system
TW: “潔利定”負壓傷口治療系統
Taiwan·Risk Class 2·Genadyne Biotechnology, Inc.·Registered Jul 17, 2015 – Jul 17, 2025ExpiredRegistration details
- Analysis ID
- b906a54b06eccbf61e45a15c5b066f6c
- Customs Code
- DHA05602750201
Company information
- Manufacturer
- Genadyne Biotechnology, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- AMED CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4780 動力式抽吸幫浦
- Import Information
- import
Dates and status
- Registration Date
- Jul 17, 2015
- Expiry Date
- Jul 17, 2025
About this record
Access comprehensive regulatory information for "Gelidine" negative pressure wound treatment system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b906a54b06eccbf61e45a15c5b066f6c and manufactured by Genadyne Biotechnology, Inc.. The authorized representative in Taiwan is AMED CO., LTD..
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