Taiwan FDA registration bfc661385d290eb146517f56b923d49e
"Kinda" Care Kit (Sterilization)
TW: 〝勤達〞護理包 (滅菌)
Registration details
- Analysis ID
- bfc661385d290eb146517f56b923d49e
- Customs Code
- DHA04600053509
Company information
- Manufacturer
- BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- TEAM POWER MEDICAL INSTRUMENT LTD.
Product details
- Intended Use
- It is limited to the first level of the medical device management measures "external use of non-absorbent gauze or sponge balls (I.4014), medical adhesive tapes and adhesive bandages (J.5240), medical absorbent fibers (J.5300), absorbent tip applicators (J.6025) and patient examination gloves (J.6250)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4014 Non-absorbent cloth or sea balls are used externally
- Import Information
- QMS/QSD;; Chinese goods;; input
Dates and status
- Registration Date
- Jul 16, 2008
- Expiry Date
- Jul 16, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kinda" Care Kit (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bfc661385d290eb146517f56b923d49e and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..
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