Taiwan FDA registration efa8c2d8b8841b91006b9137d51b2e00

ABBOTT ARCHITECT C-Peptide (Non-Sterile)

TW: 亞培設計師 C-胜肽檢驗試劑組(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BIOKIT S.A.·Registered Dec 12, 2018 – Dec 12, 2028Active
Registration details
Analysis ID
efa8c2d8b8841b91006b9137d51b2e00
License Form
Ministry of Health Medical Device Import No. 019915
Customs Code
DHA09401991508
Company information
Manufacturer
BIOKIT S.A.
Manufacturer Country
Spain
Product details
Intended Use
Limited to the first level identification range of the insulin precursor C-peptide test system (A.1135) of the management method for medical devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1135 Insulin Precursor C-Peptide Test System
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 12, 2018
Expiry Date
Dec 12, 2028
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About this record

Access comprehensive regulatory information for ABBOTT ARCHITECT C-Peptide (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 efa8c2d8b8841b91006b9137d51b2e00 and manufactured by BIOKIT S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOKIT S.A., and 1 recent registrations in the same category. 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.

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