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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
Laparoscopic tissue manipulation forceps/working-channel FDA UDI
Device Name
Snowden-Pencer MIS SUCTION IRRIGATION HANDLE SPRING CAP PACK OF 5 5/PK X 5 FDA UDI
Model / Reference
SIHSC-5 FDA UDI
Description
Snowden-Pencer MIS SUCTION IRRIGATION HANDLE SPRING CAP PACK OF 5 5/PK X 5 FDA UDI

Identifiers

Catalog Number
SIHSC5 FDA UDI
Primary DI / UDI-DI
10885403465567 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic tissue manipulation forceps/working-channel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Laparoscopic tissue manipulation forceps/working-channel

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

Similar devices

Also classified as Laparoscopic tissue manipulation forceps/working-channel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI c28b1acd-0143-4d13-aea3-2e1daf28eabb 35 fields · synced Jun 8, 2026