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Endo-Kerrison Shaft
EUDAMEDFDA UDIClass I (EU MDR)
Ref EKS24303040CU
by Joimax GmbH
Identity
- Trade Name
- Endo-Kerrison Shaft EUDAMEDEndo-Kerrison FDA UDI
- Generic Name
- Flexible endoscopic biopsy forceps, reusable FDA UDI
- Device Name
- Endo-Kerrison Shaft EUDAMEDFDA UDI
- Model / Reference
- EKS24303040CU EUDAMEDFDA UDI
- Description
- Endo-Kerrison Shaft FDA UDI
Identifiers
- Catalog Number
- EKS24303040CU FDA UDI
- Primary DI / UDI-DI
- 04250337117032 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04250337117032 EUDAMED42503371PUNCHENDWR EUDAMED
- FDA Product Code
- LRY FDA UDI
- EMDN Code
- L1199 NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Flexible endoscopic biopsy forceps, 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-Kerrison Shaft by Joimax GmbH — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-04250337117032 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-04250337117032 | 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 (3)
- EUDAMED 3412a528-e1db-446f-a15f-8dd763dd448e 61 fields · synced Jul 12, 2026
- EUDAMED f8e8c93c-1bb7-41ed-9cea-6cd70f448ace 61 fields · synced May 19, 2026
- FDA UDI b6d8c248-6ff8-4e8b-b4cd-401d83e09b13 36 fields · synced May 30, 2026