Attune 1506-10-002
Ref 1506-10-002Model ATTUNE Knee System Cemented RP Tibial Base
Active
CE MDR
Valid until
9 Jul 2029
FDA recalls
Not checked
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | NumberMDR 755208 | Date29 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10603295042563 | Date24 Mar 2015 | StatusListed |
Certificates
- MDR 755208 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 29 Jun 2026
- Expires
- 9 Jul 2029
- Reason
- Change approved
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Attune
- Generic Name
- Uncoated knee tibia prosthesis, metallic
- Device Name
- Cemented RP Tibial Base
- Model / Ref / Catalog
- 1506-10-002, ATTUNE Knee System Cemented RP Tibial Base, 150610002
- Primary DI / UDI-DI
- 10603295042563
- Basic UDI-DI
- 0603295a002578V
- FDA Product Code
- NJL
- EMDN Code
- P090903020101 Bicompartmental primary implant cemented mobile bearing tibial plates
- GMDN Term
- Uncoated knee tibia prosthesis, metallic
- Device Class
- Class III
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Conditional
Other devices from Depuy (Ireland)
Properties
Other properties (17)
- Reusable: No
- Contains Latex: No
- Reprocessed: 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
- Manufacturing Date: No