icotec Cervical Cage, Cervical Cage, Anatomic, Container Base
EUDAMEDFDA UDIClass I (EU MDR)
by icotec ag
Identity
- Trade Name
- icotec Cervical Cage, Cervical Cage, Anatomic, Container Base EUDAMEDicotec Cervical Cage, Cervical Cage Anatomic, Container Base FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- icotec Cervical Cage, Cervical Cage Anatomic, Container Base FDA UDI
- Model / Reference
- Container EUDAMED41-12-1 EUDAMEDFDA UDI
- Description
- icotec Cervical Cage, Cervical Cage Anatomic, Container Base FDA UDI
Identifiers
- Catalog Number
- 41-12-1 FDA UDI
- Primary DI / UDI-DI
- 07640164849652 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iCSI00033V EUDAMED
- Direct Marketing DI
- 07640164849652 EUDAMED
- FDA Product Code
- MAX FDA UDIODP FDA UDI
- EMDN Code
- L1109 NEUROSURGERY AND SPINAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
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
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Device sterilization/disinfection container, reusable
icotec Cervical Cage, Cervical Cage, Anatomic, Container Base by icotec AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 764017255iCSI00033V | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- icotec ag
- EUDAMED SRN
- CH-MF-000026833
- Authorised Representative
- icotec Medical GmbH DE-AR-000016837
Sources (2)
- EUDAMED 1b5f1948-f416-413d-b7a1-3e74580aa55b 61 fields · synced Jul 9, 2026
- FDA UDI 28e52f2c-16fa-4c41-8e99-c9148e5afa4d 35 fields · synced May 30, 2026