Taiwan FDA registration 6d1dadf13f3323276cb1cf9e921c4b5c
Pule supplement Rust type bone implantation
TW: 普樂補拉斯特式內植骨頭
Registration details
- Analysis ID
- 6d1dadf13f3323276cb1cf9e921c4b5c
- Customs Code
- DHA00600229502
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
- Oct 08, 1982
- Expiry Date
- Oct 08, 1987
- Cancellation Date
- Feb 26, 1990
Cancellation information
- Status
- Logged out
- Reason
- 有效期限已屆
About this record
Access comprehensive regulatory information for Pule supplement Rust type bone implantation in Taiwan's medical device market through Pure Global AI's free database. is registered under number 6d1dadf13f3323276cb1cf9e921c4b5c and manufactured by VITEK INC.. The authorized representative in Taiwan is Ming Hui Trading Company Limited.
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