Pure Global AI
EUDAMED registration 07649993414017No

Fisscure

Doc-Invent SAClass IIaEU EUDAMEDTrade name: Fisscure
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
A99
Trade name
Fisscure
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
07649993414017
Basic UDI
7649993414700001Z2
Version date
March 10, 2025
Manufacturer last update
November 06, 2024
Active status
No
Manufacturer
Manufacturer name
Doc-Invent SA
Country
Switzerland
Country type
NON_EU
Address
40 Chemin Riant-Pré Lausanne
Email
info@doc-invent.com
Authorized representative
Name
Obelis s.a.
SRN
BE-AR-000000106
Country
Belgium
Address
53 Boulevard Général Wahis Brussels
Email
regulatory@obelis.net
Telephone
+32(2)73 25 954
Regulatory information
Competent authority
Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Belgium
Market available
Belgium:2025-04-01~None, France:2025-04-01~None, Germany:2025-04-01~None, Italy:2025-04-01~None, Luxembourg:2025-04-01~None, Netherlands:2025-04-01~None, Spain:2025-04-01~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER

About this record

Access comprehensive regulatory information for Fisscure in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 07649993414017 and manufactured by Doc-Invent SA in Switzerland.

This page provides complete registration details including trade name (Fisscure), 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.