Taiwan FDA registration 25d84ea78f819dd90c3a554cf94a5666
"Ofa" Restuphao limb equipment (unsterilized)
TW: “歐法”蕾詩德寶肢體裝具 (未滅菌)
Taiwan·Risk Class 1·OFA BAMBERG GMBH·Registered Oct 14, 2008 – Oct 14, 2018CancelledRegistration details
- Analysis ID
- 25d84ea78f819dd90c3a554cf94a5666
- Customs Code
- DHA04400711700
Company information
- Manufacturer
- OFA BAMBERG GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDIBIOT CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- import
Dates and status
- Registration Date
- Oct 14, 2008
- Expiry Date
- Oct 14, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ofa" Restuphao limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25d84ea78f819dd90c3a554cf94a5666 and manufactured by OFA BAMBERG GMBH. The authorized representative in Taiwan is MEDIBIOT 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