Taiwan FDA registration 2843b499d9e612efd85028234516feba
"Tepu" safety blood collection kit
TW: “特浦”安全採血套組
Registration details
- Analysis ID
- 2843b499d9e612efd85028234516feba
- Customs Code
- DHA05603609002
Company information
- Manufacturer Country
- Malaysia;;Japan
- Authorized Representative
- TOP SURGICAL TAIWAN CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5570 Subcutaneous single-chamber needle
- Import Information
- import
Dates and status
- Registration Date
- Jan 17, 2023
- Expiry Date
- Jan 17, 2028
About this record
Access comprehensive regulatory information for "Tepu" safety blood collection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2843b499d9e612efd85028234516feba and manufactured by MEDITOP CORPORATION (M) SDN. BHD.;; TOP Corporation. The authorized representative in Taiwan is TOP SURGICAL TAIWAN CORPORATION.
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