Identity
- Trade Name
- General Instrument FDA UDI
- Generic Name
- Orthopaedic graft guide FDA UDI
- Device Name
- Battalion, LLIF Implant Slide Assy, Untracked, Long, 22mm Wide FDA UDI
- Model / Reference
- CI-10918-11 FDA UDI
- Description
- Battalion, LLIF Implant Slide Assy, Untracked, Long, 22mm Wide FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840180507568 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic graft guide 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: Orthopaedic graft guide
General Instrument by Alphatec Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic graft guide.
- Arthrex® — Arthrex, Inc. · Class I
- TC-PLUS — Smith & Nephew, Inc. · Class I
- ACE — ACE SURGICAL SUPPLY CO., INC. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · 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
- Alphatec Spine, Inc.
Sources (1)
- FDA UDI 06e8d70e-6c3f-4e44-a494-0a91c782679a 34 fields · synced Jun 8, 2026