Taiwan FDA registration e272c3b521c771e819a77d48cbe3c054
"Payon" combined laparoscopic instrument
TW: "帕永"組合式腹腔鏡用器械
Taiwan·Risk Class 2·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Oct 26, 2006 – Oct 26, 2011CancelledRegistration details
- Analysis ID
- e272c3b521c771e819a77d48cbe3c054
- Customs Code
- DHA00601738508
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Oct 26, 2006
- Expiry Date
- Oct 26, 2011
- Cancellation Date
- Nov 08, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Payon" combined laparoscopic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e272c3b521c771e819a77d48cbe3c054 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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