ATEC Light Cable System

FDA UDI

Class I (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name: ATEC Light Cable System FDA UDI
Generic Name: Open surgical site internal light FDA UDI
Device Name: LIF Illumination System, Sterile FDA UDI
Model / Reference: 169-510-S FDA UDI
Description: LIF Illumination System, Sterile FDA UDI

Identifiers

Primary DI / UDI-DI: 00190376508085 FDA UDI
FDA Product Code: FDG FDA UDI
GMDN Term: Open surgical site internal light FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 876.4530 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Open surgical site internal light

ATEC Light Cable System by Alphatec Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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NICO Myriad — NICO Corporation · 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

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Manufacturer

Manufacturer: Alphatec Spine, Inc.

Sources (1)

FDA UDI 16e557f1-23ac-421c-ae3a-302833792975 34 fields · synced Jun 8, 2026