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icotec Lumbar Cage, Slotted Hammer
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref 38-7Model Hammer
by Icotec
Identity
- Trade Name
- icotec Lumbar Cage Slotted Hammer EUDAMEDicotec Lumbar Cage, Slotted Hammer FDA UDI
- Generic Name
- Surgical mallet FDA UDI
- Device Name
- icotec Lumbar Cage, Slotted Hammer FDA UDI
- Model / Reference
- 38-7 EUDAMEDFDA UDIHammer EUDAMED
- Description
- icotec Lumbar Cage, Slotted Hammer FDA UDI
Identifiers
- Catalog Number
- 38-7 FDA UDI
- Primary DI / UDI-DI
- 07640140433363 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iLCAGE00128A EUDAMED
- Direct Marketing DI
- 07640140433363 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, Slotted Hammer 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 c28867ca-795a-4fa8-b074-035af0a2ea1e 35 fields · synced Jun 18, 2026
- EUDAMED 1b79e1dd-5c8b-46b0-827e-269c4daf875d 61 fields · synced Jun 18, 2026