EIT LLIF cage
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- CONDUIT Lateral System EUDAMEDEIT LLIF cage FDA UDI
- Generic Name
- Metallic spinal interbody fusion cage FDA UDI
- Device Name
- CONDUIT Lateral Cage EUDAMEDEIT LLIF, H 16mm, 0°, 55/26 FDA UDI
- Model / Reference
- LUI01656 EUDAMEDFDA UDICONDUIT Lateral Lumbar Interbody Fusion Cage EUDAMED
- Description
- EIT LLIF, H 16mm, 0°, 55/26 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260614033214 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a002335V EUDAMED
- FDA Product Code
- MAX FDA UDI
- EMDN Code
- P09070101 SPINAL CAGES EUDAMED
- GMDN Term
- Metallic spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
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
Yes
Manufacturing Date
Yes
Category: Metallic spinal interbody fusion cage
EIT LLIF cage by EIT Emerging Implant Technologies GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Metallic spinal interbody fusion cage.
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- MectaLIF 3D — Medacta International · Class II
- PILLAR TL — Orthofix US LLC · Class II
- Solar™ Interbody Fusion System — Degen Medical · Class II
- Peridot-TD Anterior Cervical Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
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
- EIT Emerging Implant Technologies GmbH
Sources (2)
- FDA UDI 79403527-7d79-41ee-a598-3b1794489d6e 33 fields · synced Oct 8, 2026
- EUDAMED 907f2af5-707f-4b83-b45b-4c585bbbbc0a 61 fields · synced Oct 8, 2026