Peremo-Everolimus Eluting Coronary Stent System
- Risk class
- Class III
- CND nomenclatures code
- P070402010301
- Trade name
- Peremo™
- Implantable
- Yes
- Reusable
- No
- Measuring function
- No
- Primary DI
- 18904224939018
- Basic UDI
- B-18904224939018
- Version date
- July 15, 2023
- Manufacturer last update
- June 25, 2021
- Active status
- No
- Manufacturer name
- Meril Life Sciences Pvt. Ltd.
- Country
- India
- Country type
- NON_EU
- Address
- Muktanand Marg, Chala, Vapi Vapi
- askinfo@merillfe.com
- Name
- Obelis s.a.
- SRN
- BE-AR-000000106
- Country
- Belgium
- Address
- 53 Boulevard Général Wahis Brussels
- regulatory@obelis.net
- Telephone
- +32(2)73 25 954
- Competent authority
- Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Germany
- Market available
- Germany:2018-04-27~2023-04-27, Italy:2018-04-27~2023-04-27, Netherlands:2018-04-27~2023-04-27, Spain:2018-04-27~2023-04-27
- Human tissues
- No
- Animal tissues
- No
CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS
Access comprehensive regulatory information for Peremo-Everolimus Eluting Coronary Stent System in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI 18904224939018 and manufactured by Meril Life Sciences Pvt. Ltd. in India.
This page provides complete registration details including trade name (Peremo™ ), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.