Handle Endo-Flexprobe TEFH29025
by Joimax, Inc. EUDAMEDGUDID
Active
Ref TEFH29025
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number42503371PALPENDG5 | Date29 Apr 2024 | StatusActive |
| United States | GUDID listing GUDID | Number04250337120513 | Date29 Sep 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 25 Oct 2026.
Specification
- Trade Name
- Handle Endo-Flexprobe 150 EUDAMEDHandle Endo-Flexprobe GUDID
- Generic Name
- Surgical instrument handle, non-torque-limiting
- Device Name
- Endo-Flexprobe
- Model / Ref / Catalog
- TEFH29025
- Primary DI / UDI-DI
- 04250337120513
- Basic UDI-DI
- 42503371PALPENDG5
- Direct Marketing DI
- 04250337120513
- FDA Product Code
- GFI
- EMDN Code
- L110599 Neurosurgery spreaders and retractors, reusable - other
- GMDN Term
- Surgical instrument handle, non-torque-limiting
- Device Class
- Class I
- Regulation Number
- 878.4800
- Market of Registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Joimax, Inc.
Properties
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: 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
- Serial Number: No
- Expiration Date: No