MaxMoreSpine 1001-EK 004/S
by Hoogland Spine Products, GmbH
Ref 1001-EK 004/SModel Punches
MaxMoreSpine 1001-EK 004/S is a Class I device made by Hoogland Spine Products, GmbH, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI B-04260200312969) and listed in FDA GUDID since 28 Feb 2022 (UDI-DI 04260200312969), active as of 7 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-04260200312969 04260200312969 | Date4 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04260200312969 | Date28 Feb 2022 | StatusListed |
Official records
- EUDAMED public site B-04260200312969
- AccessGUDID record 04260200312969
Across registries
- EUDAMED Basic UDI-DI B-04260200312969 registered 4 Nov 2026 Active
- FDA GUDID UDI-DI 04260200312969 listed 28 Feb 2022 Listed
Timeline
- Listed FDA GUDID 04260200312969
- Registered EUDAMED B-04260200312969
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Ceramic Coated Kerrison 4.0 mm shaft 330 mm - 40° EUDAMEDMaxMoreSpine GUDID
- Generic name
- Rigid endoscopic biopsy forceps, reusable
- Model / reference
- 1001-EK 004/S, Punches
- Primary DI / UDI-DI
- 04260200312969
- Basic UDI-DI
- B-04260200312969
- FDA product code
- LRY
- EMDN code
- L1904 Arthroscopic surgery forceps and punches, reusable
- GMDN term
- Rigid endoscopic biopsy forceps, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization