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Snowden-Pencer

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
Snowden-Pencer FDA UDI
Generic Name
Open surgical site internal light FDA UDI
Device Name
Fiber Optic Light Panel 5 inches 12.7CM FDA UDI
Model / Reference
88-1005K FDA UDI
Description
Fiber Optic Light Panel 5 inches 12.7CM FDA UDI

Identifiers

Catalog Number
881005K FDA UDI
Primary DI / UDI-DI
10885403285363 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Open surgical site internal light

Snowden-Pencer by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open surgical site internal light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI da3b04eb-9beb-4d2c-99e9-79729b0bba43 35 fields · synced Jun 8, 2026