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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
Suturing needle holder, reusable FDA UDI
Device Name
DIAMOND-JAW NEEDLE HOLDER JULIAN, 20.5CM 8 inches 4000 JAW, STRAIGHT FDA UDI
Model / Reference
32-0328 FDA UDI
Description
DIAMOND-JAW NEEDLE HOLDER JULIAN, 20.5CM 8 inches 4000 JAW, STRAIGHT FDA UDI

Identifiers

Catalog Number
320328 FDA UDI
Primary DI / UDI-DI
10885403144226 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

Yes

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: Suturing needle holder, reusable

A comprehensive hand-held manual surgical instrument designed to grasp a suture needle when pushing/pulling the needle and attached suture through tissue during suturing. It is typically made of metal and has short serrated jaws at the distal end to provide better grip of the needle.

Similar devices

Also classified as Suturing needle holder, 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 1198aea0-97a1-494c-804d-ac4903c1f9de 35 fields · synced Jul 10, 2026