Taiwan FDA registration bfc661385d290eb146517f56b923d49e

"Kinda" Care Kit (Sterilization)

TW: 〝勤達〞護理包 (滅菌)
Taiwan flagTaiwan·Risk Class 1·BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.·Registered Jul 16, 2008 – Jul 16, 2018Cancelled
Registration details
Analysis ID
bfc661385d290eb146517f56b923d49e
Customs Code
DHA04600053509
Company information
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..

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.

Free DatabasePowered by Pure Global AI89,000+ Devices