Curette, triangular
EUDAMEDFDA UDIClass I (EU MDR)
by Joimax GmbH
Identity
- Trade Name
- Curette, triangular EUDAMEDCurette EUDAMEDFDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Curette, triangular EUDAMEDFDA UDICurette EUDAMEDFDA UDI
- Model / Reference
- JTC23011 EUDAMEDFDA UDIDEC155011C EUDAMEDFDA UDI
- Description
- Curette FDA UDICurette, triangular FDA UDI
Identifiers
- Catalog Number
- DEC155011C FDA UDIJTC23011 FDA UDI
- Primary DI / UDI-DI
- 04250337112594 EUDAMEDFDA UDI04250337120544 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337112594 EUDAMED42503371ABLADIS5L EUDAMED42503371ABLACUR6H EUDAMED
- Direct Marketing DI
- 04250337120544 EUDAMED
- FDA Product Code
- FZS FDA UDI
- EMDN Code
- L1102 NEUROSURGERY SPATULAS AND DISSECTORS, REUSABLE EUDAMED
- GMDN Term
- Bone curette, 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
Single Use
No
Implantable
No
Reusable
Yes
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
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Surgical retractor/retraction system blade, reusable
Curette, triangular by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDD
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04250337112594 | Class I | Active |
| EUDAMED | European Union | CE/MDR | B-04250337112594 | 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 abe8ad03-8ce6-4b10-a2c7-bf61e1530554 61 fields · synced Jul 31, 2026
- EUDAMED 621df5c2-3699-4a42-950b-5f0ddcfbf616 61 fields · synced May 17, 2026
- FDA UDI f8dd8a07-11ef-49ee-8582-3ce10afc5c20 36 fields · synced May 29, 2026
- FDA UDI e1369e68-9850-4153-8ec6-29e97f4b4771 36 fields · synced May 30, 2026
- EUDAMED 066bffee-1bee-476d-84b7-3dd524c3350d 61 fields · synced Jul 9, 2026