Snowden-Pencer

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name: Snowden-Pencer FDA UDI
Generic Name: Suture knot pusher, reusable FDA UDI
Device Name: DIAMOND-LINE KNOT PUSHER OPEN END 5MM, 32CM DELICATE FDA UDI
Model / Reference: 88-9348 FDA UDI
Description: DIAMOND-LINE KNOT PUSHER OPEN END 5MM, 32CM DELICATE FDA UDI

Identifiers

Catalog Number: 889348 FDA UDI
Primary DI / UDI-DI: 10885403154836 FDA UDI
510(k) Number: K930667 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Suture knot pusher, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Suture knot pusher, reusable

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

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Also classified as Suture knot pusher, reusable.

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Closed Knot Pusher — Biomet Orthopedics, Inc. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
MICTEC KNOT PUSHER — SONTEC INSTRUMENTS, INC. · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Integra® Jarit® — Integra LifeSciences Production Corporation · Class II

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI 94ad7b05-48e0-4e22-be4a-640064686545 36 fields · synced Jun 8, 2026