Quip
by Brainlab SE
Ref 15502
Quip (15502) is a Class I device made by Brainlab SE, registered in EUDAMED on 28 Jul 2026 (Basic UDI-DI 4056481QuipDB) and listed in FDA GUDID since 1 Sep 2026 (UDI-DI 04056481144326), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number04056481144326 | Date1 Sep 2026 | StatusListed |
| European Union | CE/MDR EUDAMED | Number4056481QuipDB 04056481144326 | Date28 Jul 2026 | StatusActive |
Official records
- EUDAMED public site 4056481QuipDB
- AccessGUDID record 04056481144326
Across registries
- EUDAMED Basic UDI-DI 4056481QuipDB registered 28 Jul 2026 Active
- FDA GUDID UDI-DI 04056481144326 listed 1 Sep 2026 Listed
Timeline
- Registered EUDAMED 4056481QuipDB
- Listed FDA GUDID 04056481144326
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Medical image management system
- Model / reference
- 15502
- Primary DI / UDI-DI
- 04056481144326
- Basic UDI-DI
- 4056481QuipDB
- FDA product code
- LMD
- EMDN code
- Z11069080 Various digital bioimaging management instruments - hardware accessories
- GMDN term
- Medical image management system
- Device class
- Class I
- Regulation number
- 892.2020
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Manufacturer details
- EUDAMED SRN
- DE-MF-000006183
Similar devices in this category
Other devices filed under VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - HARDWARE ACCESSORIES.