Spotlight

FDA UDI

Class I (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name: SPOTLIGHT FDA UDI
Generic Name: Light source adaptor FDA UDI
Device Name: SPOTLIGHT ACCESS SYSTEM ILLUMINATED STRAIGHT PORT 21 x 70mm FDA UDI
Model / Reference: 698336651 FDA UDI
Description: SPOTLIGHT ACCESS SYSTEM ILLUMINATED STRAIGHT PORT 21 x 70mm FDA UDI

Identifiers

Catalog Number: 698336651 FDA UDI
Primary DI / UDI-DI: 10705034374550 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Light source adaptor 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

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Light source adaptor

Spotlight by Depuy Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Light source adaptor.

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Aspen® Flexible Light Handle Cover — Aspen Surgical Products, Inc. · Class II
Aspen® Flexible Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
Innomed, Inc. — Innomed, Inc. · Class II
Aspen® Rigid Light Handle Adapter — Aspen Surgical Products, Inc. · Class II
Aspen® Rigid Light Handle Adapter — Aspen Surgical Products, Inc. · 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: Depuy Spine, Inc.

Sources (1)

FDA UDI f781bd31-1b29-4159-a07e-13e799e7f82e 35 fields · synced May 30, 2026