Dilatator
by Geister Medizintechnik GmbH 37 variants
Part of a family of 156 devices: see the family page
Ref 21-0226
Dilatator (21-0226) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 405703400000002ZR), active as of 24 Oct 2026.
Active
CE MDR
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 | Number405703400000002ZR 04057034048337 | Date8 Oct 2026 | StatusActive |
Official records
- EUDAMED public site 405703400000002ZR
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Dilatator
- Model / reference
- 21-0226
- Primary DI / UDI-DI
- 04057034048337
- Basic UDI-DI
- 405703400000002ZR
- Direct marketing DI
- 04057034048337
- EMDN code
- L070802 Vascular dilators, reusable
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005461
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