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Spotlight

FDA UDI

Class II (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name
SPOTLIGHT FDA UDI
Generic Name
Endoscopic light source unit, line-powered FDA UDI
Device Name
SPOTLIGHT ACCESS SYSTEM ILLUMINATED STRAIGHT PORT 12 x 50mm FDA UDI
Model / Reference
282912050 FDA UDI
Description
SPOTLIGHT ACCESS SYSTEM ILLUMINATED STRAIGHT PORT 12 x 50mm FDA UDI

Identifiers

Catalog Number
282912050 FDA UDI
Primary DI / UDI-DI
10705034205533 FDA UDI
510(k) Number
K062814 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Endoscopic light source unit, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic light source unit, line-powered

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

Similar devices

Also classified as Endoscopic light source unit, line-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Spine, Inc.

Sources (1)

  • FDA UDI e8e7b365-788c-40e1-bf8c-05a0e86db56e 36 fields · synced May 31, 2026