Taiwan FDA registration 1b1947b863429a0cab40ba3c2ec2c037
"Xianchong" blood bag tube sealing machine (unsterilized)
TW: "先崇"血袋管封口機(未滅菌)
Registration details
- Analysis ID
- 1b1947b863429a0cab40ba3c2ec2c037
- Customs Code
- DHA04400225701
Company information
- Manufacturer
- CENTRON CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- Used to heat and seal plastic bag tubes containing blood and blood products.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9750 Heat-sealing equipment
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2005
- Expiry Date
- Dec 14, 2025
About this record
Access comprehensive regulatory information for "Xianchong" blood bag tube sealing machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b1947b863429a0cab40ba3c2ec2c037 and manufactured by CENTRON CORPORATION. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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