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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 RIGHT ANGLE DISSECTOR SINGLE-PIECE, DOUBLE ACTION 45CM, 5MM INSUL SHAFT, ROT, NON-RATCHETED FDA UDI
Model / Reference
88-8316 FDA UDI
Description
Snowden-Pencer RIGHT ANGLE DISSECTOR SINGLE-PIECE, DOUBLE ACTION 45CM, 5MM INSUL SHAFT, ROT, NON-RATCHETED FDA UDI

Identifiers

Catalog Number
888316 FDA UDI
Primary DI / UDI-DI
10885403178641 FDA UDI
510(k) Number
K925114 FDA UDI
FDA Product Code
HFI FDA UDI
GMDN Term
Laparoscopic tissue manipulation forceps/working-channel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4160 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.

Cleared under the same submission

K925114 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI b6efa641-b91f-4c4d-8e10-c71e82f6b754 36 fields · synced Jun 8, 2026