Taiwan FDA registration 6d1dadf13f3323276cb1cf9e921c4b5c

Pule supplement Rust type bone implantation

TW: 普樂補拉斯特式內植骨頭
Taiwan flagTaiwan·VITEK INC.·Registered Oct 08, 1982 – Oct 08, 1987Cancelled
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.

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