Taiwan FDA registration d1fc71d12f40c446ebef2f6f240fb5ed
"Pexix" dental surgical lamp (unsterilized)
TW: "沛克司" 牙科用手術燈(未滅菌)
Taiwan·Risk Class 1·SHANGHAI PAX MEDICAL INSTRUMENT CO., LTD.·Registered Mar 21, 2017 – Mar 21, 2027ActiveRegistration details
- Analysis ID
- d1fc71d12f40c446ebef2f6f240fb5ed
- Customs Code
- DHA09600302507
Company information
- Manufacturer
- SHANGHAI PAX MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HUNG TZE INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, dental surgical lamp (F.4630) first level recognition range.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4630 牙科用手術燈
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 21, 2017
- Expiry Date
- Mar 21, 2027
About this record
Access comprehensive regulatory information for "Pexix" dental surgical lamp (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1fc71d12f40c446ebef2f6f240fb5ed and manufactured by SHANGHAI PAX MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is HUNG TZE INTERNATIONAL 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.
Free DatabasePowered by Pure Global AI89,000+ Devices