Taiwan FDA registration 05cc4476ce67b532431ae3cc4f5233a2
Pule supplement Lassite-artificial total hearing bone
TW: 普樂補拉斯特式－人工全聽骨
Taiwan·VITEK INC.·Registered Apr 13, 1985 – Apr 13, 1990CancelledRegistration details
- Analysis ID
- 05cc4476ce67b532431ae3cc4f5233a2
- Customs Code
- DHA00600360904
Company information
- Manufacturer
- VITEK INC.
- Manufacturer Country
- United States
- Authorized Representative
- Ming Hui Trading Company Limited
Product details
- Product Type (Level 1)
- 0301 Artificial bones
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 1985
- Expiry Date
- Apr 13, 1990
- Cancellation Date
- Nov 01, 1999
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者;;改列無須辦理查驗之醫療器材
About this record
Access comprehensive regulatory information for Pule supplement Lassite-artificial total hearing bone in Taiwan's medical device market through Pure Global AI's free database. is registered under number 05cc4476ce67b532431ae3cc4f5233a2 and manufactured by VITEK INC.. The authorized representative in Taiwan is Ming Hui Trading Company Limited.
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