Taiwan FDA registration d2746c8d5a9d10e72f2ea36db52d10bf
"Peters Surgery" Katifron surgical sutures
TW: “彼得斯外科”卡蒂弗龍外科縫合線
Taiwan·Risk Class 2·PETERS SURGICAL·Registered Nov 18, 2009 – Nov 18, 2014CancelledRegistration details
- Analysis ID
- d2746c8d5a9d10e72f2ea36db52d10bf
- Customs Code
- DHA00602041501
Company information
- Manufacturer
- PETERS SURGICAL
- Manufacturer Country
- France
- Authorized Representative
- ANSON HEALTH CARE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5000 Non-absorbable polyethylene terephthalate sewing wire
- Import Information
- import
Dates and status
- Registration Date
- Nov 18, 2009
- Expiry Date
- Nov 18, 2014
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Peters Surgery" Katifron surgical sutures in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2746c8d5a9d10e72f2ea36db52d10bf and manufactured by PETERS SURGICAL. The authorized representative in Taiwan is ANSON HEALTH CARE 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