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icotec Lumbar Cage, End Cap Replacement, Plastic, Ø 30 mm
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref 38-7-2Model Hammer
by Icotec
Identity
- Trade Name
- icotec Lumbar Cage End Cap Replacement, Plastic Ø 30 mm EUDAMEDicotec Lumbar Cage, End Cap Replacement, Plastic, Ø 30 mm FDA UDI
- Generic Name
- Surgical mallet FDA UDI
- Device Name
- icotec Lumbar Cage, End Cap Replacement, Plastic, Ø 30 mm FDA UDI
- Model / Reference
- 38-7-2 EUDAMEDFDA UDIHammer EUDAMED
- Description
- icotec Lumbar Cage, End Cap Replacement, Plastic, Ø 30 mm FDA UDI
Identifiers
- Catalog Number
- 38-7-2 FDA UDI
- Primary DI / UDI-DI
- 07640164843865 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iLCAGE00128A EUDAMED
- Direct Marketing DI
- 07640164843865 EUDAMED
- FDA Product Code
- MAX FDA UDIODP FDA UDI
- EMDN Code
- L1109 NEUROSURGERY AND SPINAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
- GMDN Term
- Surgical mallet 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
Category: Surgical mallet
icotec Lumbar Cage, End Cap Replacement, Plastic, Ø 30 mm by Icotec — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Icotec
Sources (2)
- FDA UDI 9bac43fa-ec11-4ce1-9562-d5a03bcedadc 35 fields · synced Jul 18, 2026
- EUDAMED fffdcf74-8b2f-4241-a6b1-accce2488ecd 61 fields · synced Jul 18, 2026