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Snowden-Pencer

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
Snowden-Pencer FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
Snowden-Pencer MIS SCISSORS INSERT, MINI METZ 36CM, 10/BOX FDA UDI
Model / Reference
SP8302 FDA UDI
Description
Snowden-Pencer MIS SCISSORS INSERT, MINI METZ 36CM, 10/BOX FDA UDI

Identifiers

Catalog Number
SP8302 FDA UDI
Primary DI / UDI-DI
10885403184154 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand-held surgical retractor, reusable

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

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI db24e0b9-58eb-423b-be91-ac9795ba32d1 35 fields · synced Jun 8, 2026