Taiwan FDA registration 922717a2c10e5f57edcf6468da67d322

"MACOPHARMA" Portable Tube Sealer (Non-Sterile)

TW: "瑪科法馬" 攜帶式血袋管封口機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·MACOPHARMA·Registered Aug 09, 2017 – Aug 09, 2022Expired
Registration details
Analysis ID
922717a2c10e5f57edcf6468da67d322
License Form
Ministry of Health Medical Device Import No. 018159
Customs Code
DHA09401815904
Company information
Manufacturer
MACOPHARMA
Manufacturer Country
France
Authorized Representative
K2 INTERNATIONAL MEDICAL INC.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Heating and Sealing Equipment (B.9750)".
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B9750 Heat sealing equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 09, 2017
Expiry Date
Aug 09, 2022
About this record

Access comprehensive regulatory information for "MACOPHARMA" Portable Tube Sealer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 922717a2c10e5f57edcf6468da67d322 and manufactured by MACOPHARMA. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..

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