Axsos 703562
Ref 703562Model 08858251002553SY
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number08858251002553SY 04546540693891 | Date2 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04546540693891 | Date24 Sep 2016 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Axsos
- Generic Name
- Orthopaedic implant-instrument extension adaptor, reusable
- Device Name
- Axsos Instruments - Handles and Adaptors - Class I - Reusable - Non Sterile
- Model / Ref / Catalog
- 703562, 08858251002553SY
- Primary DI / UDI-DI
- 04546540693891
- Basic UDI-DI
- 08858251002553SY
- Direct Marketing DI
- 04546540693891
- FDA Product Code
- HWC, HRS
- EMDN Code
- P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
- GMDN Term
- Orthopaedic implant-instrument extension adaptor, reusable
- Device Class
- Class I EUDAMEDClass II GUDID
- Regulation Number
- 888.3040, 888.3030
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class I | Class II |
Other devices from Stryker Corp.
Properties
Other properties (20)
- Sterile: No
- Single Use: No
- 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
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No