Coated VICRYL
by Johnson & Johnson International 640 variants
Ref V7820EModel VICRYL Suture
Active
CE MDR
Valid until
15 Dec 2027
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number0705031a0113046 10705031109834 | Date23 Dec 2025 | StatusActive |
Certificates
- MDR 730029 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 21 Aug 2026
- Expires
- 15 Dec 2027
- Reason
- Other
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- VICRYL Suture
- Model / reference
- VICRYL Suture, V7820E
- Primary DI / UDI-DI
- 10705031109834
- Basic UDI-DI
- 0705031a0113046
- EMDN code
- H010101020201, H010101020202
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- BE-MF-000008018
Other devices from Johnson & Johnson International
Properties
Other properties (12)
- Sterilise before use: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No