Taiwan FDA registration eb17ba977822588d88bb62d956f77450
“HEBU”Cast Removal Instrument (Non-Sterile)
TW: “赫柏”石膏拆除器械 (未滅菌)
Registration details
- Analysis ID
- eb17ba977822588d88bb62d956f77450
- License Form
- Ministry of Health Medical Device Import No. 021681
- Customs Code
- DHA09402168101
Company information
- Manufacturer
- HEBU MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Shiang Tai Medical Instructment CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Gypsum Removal Devices (N.5960)".
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N5960 Gypsum removal apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 01, 2020
- Expiry Date
- Jul 01, 2025
About this record
Access comprehensive regulatory information for “HEBU”Cast Removal Instrument (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 eb17ba977822588d88bb62d956f77450 and manufactured by HEBU MEDICAL GMBH. The authorized representative in Taiwan is Shiang Tai Medical Instructment 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