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Devon

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Devon FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
Needle Counter, 1930 Foam Block FDA UDI
Model / Reference
31142378 FDA UDI
Description
Needle Counter, 1930 Foam Block FDA UDI

Identifiers

Catalog Number
31142378 FDA UDI
Primary DI / UDI-DI
10192253052282 FDA UDI
FDA Product Code
GAB FDA UDI
GMDN Term
Suturing needle holder, 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suturing needle holder, reusable

Devon by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI 8cb3c16f-793d-4054-be5b-8e5015902c4f 34 fields · synced Jun 6, 2026