Taiwan FDA registration 155fa09da95dc70a3c38393a65d510d3
Kamikioi OK Kizuna (unsterilized)
TW: 上潔OK絆(未滅菌)
Registration details
- Analysis ID
- 155fa09da95dc70a3c38393a65d510d3
- Customs Code
- DHY04300137307
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PIIN JIH CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5240 Adhesive tapes and adhesive bandages for medical use
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- May 16, 2006
- Expiry Date
- May 16, 2011
- Cancellation Date
- Nov 09, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kamikioi OK Kizuna (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 155fa09da95dc70a3c38393a65d510d3 and manufactured by Venice Pharmaceutical Factory Ltd;; Pinki Limited. The authorized representative in Taiwan is PIIN JIH 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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