Taiwan FDA registration 16ff36557986791d33101a0aec7764ab
"Bayman" Arthroscopy Accessories (Unsterilized)
TW: "貝曼" 關節鏡 附件 (未滅菌)
Taiwan·Risk Class 1·BEMA GMBH CO. KG·Registered Apr 13, 2006 – Apr 13, 2011CancelledRegistration details
- Analysis ID
- 16ff36557986791d33101a0aec7764ab
- Customs Code
- DHA04400376907
Company information
- Manufacturer
- BEMA GMBH CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- Liren Equipment Factory Co., Ltd
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 Orthopedics
- Product Type (Level 2)
- N.1100 Closing Lenses
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2006
- Expiry Date
- Apr 13, 2011
- Cancellation Date
- Jan 17, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayman" Arthroscopy Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 16ff36557986791d33101a0aec7764ab and manufactured by BEMA GMBH CO. KG. The authorized representative in Taiwan is Liren Equipment Factory 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