icotec Lumbar Cage Bone Tamper
EUDAMEDFDA UDIClass I (EU MDR)
by icotec ag
Identity
- Trade Name
- icotec Lumbar Cage Bone Tamper EUDAMEDicotec Lumbar Cage, Bone Tamper FDA UDI
- Generic Name
- Surgical tamp, reusable FDA UDI
- Device Name
- icotec Lumbar Cage, Bone Tamper FDA UDI
- Model / Reference
- Bone Tamper EUDAMED38-033 EUDAMEDFDA UDI
- Description
- icotec Lumbar Cage, Bone Tamper FDA UDI
Identifiers
- Catalog Number
- 38-033 FDA UDI
- Primary DI / UDI-DI
- 07640164841809 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iLCAGE00088K EUDAMED
- Direct Marketing DI
- 07640164841809 EUDAMED
- FDA Product Code
- MAX FDA UDIODP FDA UDI
- EMDN Code
- L1109 NEUROSURGERY AND SPINAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
- GMDN Term
- Surgical tamp, 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 Lumbar Cage Bone Tamper by icotec AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Device sterilization/disinfection container, reusable.
- SM - LIPO PANTY CHEVILLES COUPE TAILLE NOIR AVEC TROUS RECOUVERTS SUR MESURE — MEDICAL Z · Class I
- APTUS — Medartis Inc. · Class I
- APTUS — Medartis Inc. · Class II
- INSTRUMENTS TRAYS WITHOUT LID, 200x100x25MM — DAUD JEE MFG. CO · Class I
- Breastform Cover Right Size 03 (478/ 482) — Trulife · Class I
- NCB® Periprosthetic Plate System — Zimmer, Inc. · Class I
- NTOC cassette — NTOC medische techniek B.V · Class I
- MIRABOR-CA (12 BURS)- — Hager Worldwide, Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 764017255iLCAGE00088K | 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 7a628b03-1372-4191-9eaf-390b2dfd1429 61 fields · synced Jul 17, 2026
- FDA UDI 669cc984-54b4-448b-8eb7-24424597f2ee 35 fields · synced May 30, 2026