Peru DIGEMID registration DMDIV0922E
RECOMLINE.
Device classification
- Product Type
- IN VITRO MEDICAL DEVICE
Registration information
- Analysis ID
- DMDIV0922E
- Registration Date
- April 03, 2014
- Expiration Date
- April 03, 2029
- Creation Date
- March 10, 2025
Manufacturer
- Name
- MIKROGEN GmbH
Authorized Representative
- Name
- VIKMAR S.A.C.
About this record
Access comprehensive regulatory information for RECOMLINE. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DMDIV0922E and manufactured by MIKROGEN GmbH. The device was registered on April 03, 2014.
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.
Free DatabasePowered by Pure Global AIDIGEMID Official Data