← Back to catalogue
icotec Lumbar Cage Implant Holder for Tamping
EUDAMEDFDA UDIClass I (EU MDR)
Ref 38-036Model Implant Holder
by icotec ag
Identity
- Trade Name
- icotec Lumbar Cage Implant Holder for Tamping EUDAMEDicotec Lumbar Cage, Implant Holder for Tamping FDA UDI
- Generic Name
- Bone graft packing block FDA UDI
- Device Name
- icotec Lumbar Cage, Implant Holder for Tamping FDA UDI
- Model / Reference
- Implant Holder EUDAMED38-036 EUDAMEDFDA UDI
- Description
- icotec Lumbar Cage, Implant Holder for Tamping FDA UDI
Identifiers
- Catalog Number
- 38-036 FDA UDI
- Primary DI / UDI-DI
- 07640164841830 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iLCAGE001086 EUDAMED
- Direct Marketing DI
- 07640164841830 EUDAMED
- FDA Product Code
- MAX FDA UDIODP FDA UDI
- EMDN Code
- L1112 NEUROSURGERY SUCTION CANNULAS, REUSABLE EUDAMED
- GMDN Term
- Bone graft packing block 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
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
No
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
icotec Lumbar Cage Implant Holder for Tamping by icotec AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 764017255iLCAGE001086 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- icotec ag
- EUDAMED SRN
- CH-MF-000026833
- Authorised Representative
- icotec Medical GmbH DE-AR-000016837
Sources (2)
- EUDAMED 0969d859-9751-43ee-bfb2-7b2758d90936 61 fields · synced Sep 18, 2026
- FDA UDI 32ee54c3-f613-4bd6-9761-ccf880d0c19b 35 fields · synced May 30, 2026