Taiwan FDA registration 7e23d5f3fe32ebfaf670b2993c26ede0
- Pule supplemented Lassiter-type manual transplantation surgical materials
TW: －普樂補拉斯特式人工移式人工移植手術材料
Taiwan·VITEK INC.·Registered Mar 10, 1982 – Mar 10, 1991CancelledRegistration details
- Analysis ID
- 7e23d5f3fe32ebfaf670b2993c26ede0
- Customs Code
- DHA00600192504
Company information
- Manufacturer
- VITEK INC.
- Manufacturer Country
- United States
- Authorized Representative
- Ming Hui Trading Company Limited
Product details
- Product Type (Level 1)
- 0329 Artificial materials are implanted
- Import Information
- import
Dates and status
- Registration Date
- Mar 10, 1982
- Expiry Date
- Mar 10, 1991
- Cancellation Date
- Nov 01, 1999
Cancellation information
- Status
- Logged out
- Reason
- 改列無須辦理查驗之醫療器材;;未展延而逾期者
About this record
Access comprehensive regulatory information for - Pule supplemented Lassiter-type manual transplantation surgical materials in Taiwan's medical device market through Pure Global AI's free database. is registered under number 7e23d5f3fe32ebfaf670b2993c26ede0 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