← Back to catalogue

Snowden-Pencer

FDA UDI

Class I (US FDA UDI)

by Carefusion 2200, Inc.

Identity

Trade Name
Snowden-Pencer FDA UDI
Generic Name
Soft-tissue surgical hook, reusable FDA UDI
Device Name
Snowden-Pencer HOOKS MILLARD THIMBLE DOUBLE HOOK, 21MM WIDE FDA UDI
Model / Reference
88-1520 FDA UDI
Description
Snowden-Pencer HOOKS MILLARD THIMBLE DOUBLE HOOK, 21MM WIDE FDA UDI

Identifiers

Catalog Number
88-1520 FDA UDI
Primary DI / UDI-DI
10885403151941 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Soft-tissue surgical hook, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9b220b60-584e-4fd8-9ae8-495160b1cbf6 36 fields · synced Sep 18, 2026