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Snowden-Pencer

FDA UDI

Class I (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
Snowden-Pencer FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
Snowden-Pencer Plastics DIAMOND-LITE SCISSORS TITANIUM MICRO, FLAT HANDLE 14CM (5-1/2"), STRAIGHT FDA UDI
Model / Reference
32-4605 FDA UDI
Description
Snowden-Pencer Plastics DIAMOND-LITE SCISSORS TITANIUM MICRO, FLAT HANDLE 14CM (5-1/2"), STRAIGHT FDA UDI

Identifiers

Catalog Number
32-4605 FDA UDI
Primary DI / UDI-DI
10885403147142 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 FDA UDI
Commercial Distribution
Not 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

Snowden-Pencer by Carefusion 2200, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 37035778-587b-476f-923e-9fc1061a8db8 36 fields · synced Sep 18, 2026