CombiScreen® DIP Check - ARCSA Registration eff11a5e1a28ce2799612bf74831c8fa
Access comprehensive regulatory information for CombiScreen® DIP Check in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID eff11a5e1a28ce2799612bf74831c8fa and manufactured by ANALYTICON BIOTECHNOLOGIES GMBH. The device was registered on January 27, 2020.
This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
II
eff11a5e1a28ce2799612bf74831c8fa
CombiScreen® DIP Check
ARCSA ID: eff11a5e1a28ce2799612bf74831c8fa
Device Classification
Risk Class
II
Product Type
In Vitro Diagnostic
Brand Name
ANALYTICON
Commercial Name
17-480. IVD Reagents/Kits, Clinical Chemistry, Rapid Assay, Urine
Registration Information
Analysis ID
eff11a5e1a28ce2799612bf74831c8fa
Registration Date
January 27, 2020
Expiration Date
January 27, 2025
Product Use
QUALITY CONTROL TESTED FOR VARIOUS URINALYSIS TEST STRIPS AND QUALITATIVE HCG METHODS.
Manufacturer
Product Owner
Name
ANALYTICON BIOTECHNOLOGIES GMBH
Country
GERMANY
Authorized Representative