Axis Spine Technologies ALIF Implant

FDA UDI

Class II (US FDA UDI)

by Axis Spine Technologies Ltd

Identity

Trade Name: Axis Spine Technologies ALIF Implant FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Device Name: ALIF Bone Screw Tapered - 22.5mm FDA UDI
Model / Reference: 1984-52-225 FDA UDI
Description: ALIF Bone Screw Tapered - 22.5mm FDA UDI

Identifiers

Catalog Number: 1984-52-225 FDA UDI
Primary DI / UDI-DI: 05056619801236 FDA UDI
FDA Product Code: OVD FDA UDI
GMDN Term: Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Metallic spinal interbody fusion cage

Axis Spine Technologies ALIF Implant by Axis Spine Technologies Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Axis Spine Technologies Ltd

Sources (1)

FDA UDI 62d2fceb-2ffd-4081-b842-f7e09267605d 35 fields · synced Jun 6, 2026