QUICKGEL SPLIT BETA SPE KIT, QUICKGEL IFE KIT. - DIGEMID Registration DMDIV3549E
Access comprehensive regulatory information for QUICKGEL SPLIT BETA SPE KIT, QUICKGEL IFE KIT. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV3549E and manufactured by HELENA LABORATORIES, CORP.. The device was registered on September 24, 2020.
This page provides complete registration details including product type (IN VITRO MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.
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DIGEMID Official Data
DMDIV3549E
QUICKGEL SPLIT BETA SPE KIT, QUICKGEL IFE KIT.
DIGEMID ID: DMDIV3549E
Device Classification
Product Type
IN VITRO MEDICAL DEVICE
Registration Information
Analysis ID
DMDIV3549E
Registration Date
September 24, 2020
Expiration Date
September 24, 2025
Creation Date
March 10, 2025
Manufacturer
Authorized Representative

