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Endo-Elevator blunt, without Handle
EUDAMEDFDA UDIClass I (EU MDR)
Ref TEE372620Ref JDA323515.
by Joimax GmbH
Identity
- Trade Name
- Endo-Elevator blunt, without Handle EUDAMEDendo-elevator blunt FDA UDIelevator FDA UDI
- Generic Name
- Bone lever/elevator, reusable FDA UDI
- Device Name
- Endo-Elevator blunt EUDAMEDEndo-Elevator blunt, without Handle EUDAMEDFDA UDIElevator EUDAMED
- Model / Reference
- TEE372620 EUDAMEDFDA UDIJDA323515. EUDAMEDFDA UDI
- Description
- Endo-Elevator blunt, without Handle FDA UDI
Identifiers
- Catalog Number
- JDA323515. FDA UDITEE372620 FDA UDI
- Primary DI / UDI-DI
- 04250337101178 EUDAMEDFDA UDI04250337116738 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371PALPEXAGV EUDAMEDB-04250337101178 EUDAMED42503371PALPELEFZ EUDAMED
- Direct Marketing DI
- 04250337116738 EUDAMED
- FDA Product Code
- GEG FDA UDI
- EMDN Code
- L110599 NEUROSURGERY SPREADERS AND RETRACTORS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Bone lever/elevator, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Endo-Elevator blunt, without Handle by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 42503371PALPEXAGV | Class I | Active |
| EUDAMED | European Union | CE/MDR | 42503371PALPEXAGV | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (5)
- EUDAMED 6521a8d2-b49b-4929-81ef-0755b69ba928 61 fields · synced Jul 31, 2026
- EUDAMED 23ffa3d5-cd03-474e-8630-24d8aedc5b72 61 fields · synced May 19, 2026
- FDA UDI bf70b1d6-fd33-4e32-8f5f-a243e44e1dbd 36 fields · synced May 30, 2026
- FDA UDI 615e2b35-7198-4e5d-8290-89f484648271 36 fields · synced May 30, 2026
- EUDAMED ec04ab89-07b4-488c-84b5-641c991160be 61 fields · synced Jul 31, 2026