Identity
- Trade Name
- Kerrison FDA UDI
- Generic Name
- Spinal endoscopic-access system FDA UDI
- Model / Reference
- 12-1945 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00846338003722 FDA UDI
- FDA Product Code
- LRY FDA UDI
- GMDN Term
- Spinal endoscopic-access system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Spinal endoscopic-access system
Kerrison by Elliquence Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spinal endoscopic-access system.
- joimax® — JOIMAX, INC. · Class II
- Medtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC. · Class II
- OptiLIF Endo, Direct Visualization System — SPINEOLOGY INC. · Class I
- MaxView™ System - Posterior Set — VISEON, INC. · Class II
- Medfix — Medfix International, LLC · Class I
- Medfix — Medfix International, LLC · Class I
- Medfix — Medfix International, LLC · Class I
- ENDOSPINE — Karl Storz GmbH & Co. KG · Class II
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
- Elliquence Llc
Sources (1)
- FDA UDI 8dd6b7bc-0df3-42e5-91d9-d5898d36b31b 32 fields · synced May 30, 2026