Taiwan FDA registration 01c219111c0c4e482eba0b46ecceca25
Titanium ossicle segment and hand bone joint system
TW: 鈦金屬小骨段及手部骨接合術系統
Registration details
- Analysis ID
- 01c219111c0c4e482eba0b46ecceca25
- Customs Code
- DHA00600609501
Company information
- Manufacturer
- STRYKER LEIBINGER GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- Nanye Enterprise Co., Ltd
Product details
- Product Type (Level 1)
- 0399 Other artificial function substitutes
- Import Information
- import
Dates and status
- Registration Date
- Oct 17, 1990
- Expiry Date
- Oct 17, 1995
- Cancellation Date
- Sep 13, 2000
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Titanium ossicle segment and hand bone joint system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 01c219111c0c4e482eba0b46ecceca25 and manufactured by STRYKER LEIBINGER GMBH & CO. KG. The authorized representative in Taiwan is Nanye Enterprise 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