Peru DIGEMID registration DM3708E
RESTYLANE® LYFT LIDOCAINE, MARCA: RESTYLANE®
Device classification
- Product Type
- MEDICAL DEVICE
Registration information
- Analysis ID
- DM3708E
- Registration Date
- December 16, 2013
- Expiration Date
- December 16, 2023
- Creation Date
- August 12, 2024
Manufacturer
- Name
- Q-MED AB
Authorized Representative
About this record
Access comprehensive regulatory information for RESTYLANE® LYFT LIDOCAINE, MARCA: RESTYLANE® in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM3708E and manufactured by Q-MED AB. The device was registered on December 16, 2013.
This page provides complete registration details including product type (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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