EndoWrist Stapler Release Kit, Finnish
Ref 381384
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number08868741201637K 00886874113332 | Date4 Jun 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Stapler Release Kit
- Model / Reference
- 381384
- Primary DI / UDI-DI
- 00886874113332
- Basic UDI-DI
- 08868741201637K
- Direct Marketing DI
- 00886874113332
- EMDN Code
- V9099 Various devices not included in other classes - other
- Device Class
- Class I
- Market of Registration
- Finland
Manufacturer details
- EUDAMED SRN
- US-MF-000020711
- Authorised representative
- Intuitive Surgical SAS FR-AR-000009053
Other devices from Intuitive Surgical, Inc.
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- 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