Taiwan FDA registration 855d92254ade7c7a544e4698f0934425

Meiril capillary blood collection tube (unsterilized)

TW: 美艾利爾毛細血液採集管(未滅菌)
Taiwan flagTaiwan·Risk Class 1·ALERE SAN DIEGO, INC.·Registered Dec 02, 2010 – Dec 02, 2020Cancelled
Registration details
Analysis ID
855d92254ade7c7a544e4698f0934425
Customs Code
DHA04400960201
Company information
Manufacturer Country
United States
Authorized Representative
Abbott Rapid Diagnostics Health Corp.
Product details
Intended Use
Limited to the first level identification range of "Capillary Blood Collection Tube (B.6150)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.6150 Capillary Blood Collection Tubes
Import Information
import
Dates and status
Registration Date
Dec 02, 2010
Expiry Date
Dec 02, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for Meiril capillary blood collection tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 855d92254ade7c7a544e4698f0934425 and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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