Taiwan FDA registration a0fe3523b74ad1e7af05bec3d495e38a
"Nishibi" electric hemostatic device
TW: "西美" 電動止血器
Registration details
- Analysis ID
- a0fe3523b74ad1e7af05bec3d495e38a
- Customs Code
- DHA00601119206
Company information
- Manufacturer
- ZIMMER SURGICAL,INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Zimmer Medical Device Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2005
- Expiry Date
- Apr 13, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nishibi" electric hemostatic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0fe3523b74ad1e7af05bec3d495e38a and manufactured by ZIMMER SURGICAL,INC.. The authorized representative in Taiwan is Taiwan Zimmer Medical Device 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