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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
General-purpose surgical scissors, reusable FDA UDI
Device Name
Snowden-Pencer Plastics DIAMOND-EDGES SCISSORS MAYO-CARROLL 23CM 9 inches, CURVED FDA UDI
Model / Reference
32-0860 FDA UDI
Description
Snowden-Pencer Plastics DIAMOND-EDGES SCISSORS MAYO-CARROLL 23CM 9 inches, CURVED FDA UDI

Identifiers

Catalog Number
320860 FDA UDI
Primary DI / UDI-DI
10885403145858 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: General-purpose surgical scissors, reusable

The Snowden-Pencer Plastics DIAMOND-EDGES SCISSORS are a general-purpose surgical scissors designed for cutting and dissecting various tissues during open surgery. They feature pivoted shearing blades with handles, allowing for precise control and ease of use.

Similar devices

Also classified as General-purpose surgical scissors, 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 5883ff4d-33fb-4057-96af-3931be166735 35 fields · synced Jun 25, 2026