Apex®
Ref 5057-6-101SModel 08858251002803SY
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number08858251002803SY 07613327455854 | Date28 Jul 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Apex Instruments - Opening Instrumentation - Class I - Reusable - Sterile
- Model / Reference
- 08858251002803SY, 5057-6-101S
- Primary DI / UDI-DI
- 07613327455854
- Basic UDI-DI
- 08858251002803SY
- Direct Marketing DI
- 07613327455854
- EMDN Code
- P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
- Device Class
- Class I
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- CH-MF-000009332
- Authorised representative
- Stryker European Operations Limited IE-AR-000000092
Other devices from Stryker GmbH
Properties
Other properties (10)
- Implantable: 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