BEE PLIF Cage 7 x 24 mm 0°
Ref BLP0724L00
Active
CE MDR
Valid until
10 Sep 2029
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number20397GB450260529 | Date29 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04251631410966 | Date11 Jul 2022 | StatusListed |
Certificates
- 20397GB450260529 Active
Technical documentation EU MDR
- Certifier
- DNV MEDCERT GmbH 0482
- Issued
- 29 May 2026
- Expires
- 10 Sep 2029
- Reason
- Add device or group
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- BEE PLIF Cage 07 x 24 mm 0° EUDAMEDBEE PLIF Cage GUDID
- Generic Name
- Metallic spinal interbody fusion cage
- Device Name
- "BEE PLIF Cage" and "NGM WAVE PLIF Cage"
- Model / Ref / Catalog
- BLP0724L00, 7 x 24 mm 0°
- Primary DI / UDI-DI
- 04251631410966
- Basic UDI-DI
- 42516314TD026III52
- 510(k) Number
- FDA Product Code
- MAX
- EMDN Code
- P09070101 Spinal cages
- GMDN Term
- Metallic spinal interbody fusion cage
- Device Class
- Class III EUDAMEDClass II GUDID
- Regulation Number
- 888.3080
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / Reference | BLP0724L00 | 7 x 24 mm 0° |
| Device Class | Class III | Class II |
Other devices from NGMedical GmbH
Properties
Other properties (17)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No