Taiwan FDA registration d48384d39504c3f6c787fcd95e800668
"Integra" Jarit Manual surgical instrument for general use (Non-Sterile)
TW: "殷特歌爾" 潔瑞一般手術用手動式器械 (未滅菌)
Registration details
- Analysis ID
- d48384d39504c3f6c787fcd95e800668
- License Form
- Ministry of Health Medical Device Import No. 016281
- Customs Code
- DHA09401628104
Company information
- Manufacturer
- INTEGRA YORK PA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- KINDMED CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 21, 2016
- Expiry Date
- Mar 21, 2021
About this record
Access comprehensive regulatory information for "Integra" Jarit Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d48384d39504c3f6c787fcd95e800668 and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is KINDMED CORPORATION.
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