Procedure pack
by GRI Medical & Electronic Technology Co., Ltd. 51 variants
Ref VMEL011Model NEU-02
Procedure pack (VMEL011) is a Class IIa device made by GRI Medical & Electronic Technology Co., Ltd., registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI B-16931918161440), active as of 7 Nov 2026.
Active
CE MDR CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberB-16931918161440 16931918161440 | Date30 Sep 2026 | StatusActive |
| European Union | CE/MDD | NumberB-16931918161440 16931918161440 | Date30 Sep 2026 | StatusActive |
Official records
- EUDAMED public site B-16931918161440
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Device name
- Procedure pack
- Model / reference
- VMEL011, NEU-02
- Primary DI / UDI-DI
- 16931918161440
- Basic UDI-DI
- B-16931918161440, 69319181F120KU
- EMDN code
- V0599 Clinical procedures kits not included in other classes - other
- Device class
- Class IIa
- System or procedure pack
- Procedure pack which is a device in itselfProcedure pack
- EU registration type
- Legacy device (under a directive)System or procedure pack
- EU market of registration
- Netherlands
- Medical purpose
- The indications for use of Procedure packs will be determined by the physician based upon the specific type of procedure and products required to perform the procedure.
Manufacturer details
- EUDAMED SRN
- CN-MF-000004203
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
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