Lumbar Interbody Fusion System (OLLIF) 30mm Implant Caddy

FDA UDI

Class I (US FDA UDI)

by Advanced Research Medical Llc

Identity

Trade Name: Lumbar Interbody Fusion System (OLLIF) 30mm Implant Caddy FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: Lumbar Interbody Fusion System (OLLIF) 30mm Implant Caddy FDA UDI
Model / Reference: ARM 1900-600 FDA UDI
Description: Lumbar Interbody Fusion System (OLLIF) 30mm Implant Caddy FDA UDI

Identifiers

Catalog Number: ARM 1900-600 FDA UDI
Primary DI / UDI-DI: 00850014575571 FDA UDI
FDA Product Code: LRP FDA UDI
GMDN Term: Instrument tray, reusable 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

FDA UDI

Single Use

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument tray, reusable

Lumbar Interbody Fusion System (OLLIF) 30mm Implant Caddy by Advanced Research Medical Llc — Class I — FDA UDI — listed in FDA GUDID

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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 I	Pending data

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Manufacturer

Manufacturer: Advanced Research Medical Llc

Sources (1)

FDA UDI af53c6cc-fc45-4eb1-942a-c1e561bdd8de 35 fields · synced May 31, 2026