Taiwan FDA registration 5a7297126a486bc1bc2349a59eb361ab
“SCHOLLY” Arthroscope instruments (Non-Sterile)
TW: “修力” 手動式關節鏡器材 (未滅菌)
Taiwan·Risk Class 1·MD·SCHOLLY FIBEROPTIC GMBH·Registered Feb 17, 2017 – Feb 17, 2022ExpiredRegistration details
- Analysis ID
- 5a7297126a486bc1bc2349a59eb361ab
- License Form
- Ministry of Health Medical Device Import No. 017504
- Customs Code
- DHA09401750403
Company information
- Manufacturer
- SCHOLLY FIBEROPTIC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2017
- Expiry Date
- Feb 17, 2022
About this record
Access comprehensive regulatory information for “SCHOLLY” Arthroscope instruments (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 5a7297126a486bc1bc2349a59eb361ab and manufactured by SCHOLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is REVO LASER 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