Identity
- Trade Name
- Medtronic Reusable Instruments FDA UDI
- Generic Name
- Bone graft funnel FDA UDI
- Device Name
- CASE 9560700 METRX LARGE TUBES CASE FDA UDI
- Model / Reference
- 9560700 FDA UDI
- Description
- CASE 9560700 METRX LARGE TUBES CASE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00721902402845 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone graft funnel FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone graft funnel
Medtronic Reusable Instruments by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone graft funnel.
- KOHDENT — Kohler Medizintechnik GmbH & Co. KG · Class I
- HiJAK™ Cervical — ATLAS SPINE INC. · Class II
- KOHDENT — Kohler Medizintechnik GmbH & Co. KG · Class I
- EquiLOX Lumbar Expandable Cage - Bone Graft Funnel — Captiva Spine · Class I
- Solus — ALPHATEC SPINE, INC. · Class I
- Life Instruments — Life Instrument Corporation · Class I
- Axis Spine Technologies ALIF System Instrument — AXIS SPINE TECHNOLOGIES LTD · Class II
- Tranquil-L™ — NEXUS SPINE, L.L.C. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| 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
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI 5a510035-e4f0-4a0c-96b2-9f939f18efd2 34 fields · synced Jun 8, 2026