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Petfine Autoject 2

FDA UDI

Class II (US FDA UDI)

by Owen Mumford Usa Incorporated

Identity

Trade Name
Petfine Autoject 2 FDA UDI
Generic Name
Syringe-loaded medication/vaccine injector, manual, professional FDA UDI
Device Name
Autoinjector FDA UDI
Model / Reference
AJ 3310VET FDA UDI
Description
Autoinjector FDA UDI

Identifiers

Primary DI / UDI-DI
00384703310018 FDA UDI
510(k) Number
K945660 FDA UDI
FDA Product Code
KZH FDA UDI
GMDN Term
Syringe-loaded medication/vaccine injector, manual, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6920 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 25 Millimeter FDA UDI
Length — 210 Millimeter FDA UDI

Category: Syringe-loaded medication/vaccine injector, manual, professional

Petfine Autoject 2 by Owen Mumford Usa Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Syringe-loaded medication/vaccine injector, manual, professional.

Cleared under the same submission

K945660 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Owen Mumford Usa Incorporated

Sources (1)

  • FDA UDI b0cb707d-0dd2-4374-9896-890dee0674d2 37 fields · synced May 30, 2026