Taiwan FDA registration 18cdd29db98def9511f0b7575f19fbb2
Venice PU OK繃 (未滅菌)
Registration details
- Analysis ID
- 18cdd29db98def9511f0b7575f19fbb2
- Customs Code
- DHY04300044300
Company information
- Manufacturer
- VENICE LABORATORIES CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- VENICE LABORATORIES CO., LTD.
Product details
- Intended Use
- It is used to cover and protect the wound and to join the skin wound.
- 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
Dates and status
- Registration Date
- Oct 24, 2005
- Expiry Date
- Oct 24, 2025
About this record
Access comprehensive regulatory information for Venice PU OK繃 (未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18cdd29db98def9511f0b7575f19fbb2 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES 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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