ProGripTM
by Sofradim Production 8 variants
Ref TMP3008G
ProGripTM (TMP3008G) is a Class III device made by Sofradim Production, registered in EUDAMED on 20 Jul 2026 (Basic UDI-DI 0763000B00026548H) with CE/MDR certificate MDR 729718 valid until 20 Feb 2028, active as of 24 Oct 2026.
Active
CE MDR
Valid until
20 Feb 2028
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberMDR 729718 | Date11 Aug 2026 | StatusActive |
Official records
- EUDAMED public site 0763000B00026548H
Certificates
- MDR 729718 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 11 Aug 2026
- Expires
- 20 Feb 2028
- Reason
- Change approved
- MDR 729718 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 30 Jun 2026
- Expires
- 20 Feb 2028
- Reason
- Change approved
Timeline
- Registered EUDAMED 0763000B00026548H
- Certificate issued EUDAMED MDR 729718
- Certificate expires EUDAMED MDR 729718
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
- Austria
- Belgium
- Bulgaria
- Croatia
- Cyprus
- Czechia
- Denmark
- Estonia
- Finland
- France
- Germany
- Greece
- Hungary
- Iceland
- Ireland
- Italy
- Latvia
- Liechtenstein
- Lithuania
- Luxembourg
- Malta
- Netherlands
- Norway
- Poland
- Portugal
- Romania
- Slovakia
- Slovenia
- Spain
- Sweden
- Türkiye
Specification
- Device name
- ProGrip self Gripping polyester Mesh
- Model / reference
- TMP3008G
- Primary DI / UDI-DI
- 10884521780613
- Basic UDI-DI
- 0763000B00026548H
- EMDN code
- P900204 Surgical meshes, more than one component
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000012211
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