Taiwan FDA registration 2839679bbf31a5cf0e3622b346ba794e
"Gleich" dental hand instruments (unsterilized)
TW: "格利希" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·QURESHI MANUFACTURING CORPORATION·Registered May 24, 2011 – May 24, 2026ExpiredRegistration details
- Analysis ID
- 2839679bbf31a5cf0e3622b346ba794e
- Customs Code
- DHA04401039305
Company information
- Manufacturer
- QURESHI MANUFACTURING CORPORATION
- Manufacturer Country
- Pakistan
- Authorized Representative
- ADVANCE DEVELOPMENT INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- May 24, 2011
- Expiry Date
- May 24, 2026
About this record
Access comprehensive regulatory information for "Gleich" dental hand instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2839679bbf31a5cf0e3622b346ba794e and manufactured by QURESHI MANUFACTURING CORPORATION. The authorized representative in Taiwan is ADVANCE DEVELOPMENT 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