Injekt®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name: Injekt® FDA UDI
Generic Name: Metered-delivery hypodermic syringe FDA UDI
Device Name: Injekt®-F (1 ml) (9166017V) FDA UDI
Model / Reference: 9166017V FDA UDI
Description: Injekt®-F (1 ml) (9166017V) FDA UDI

Identifiers

Catalog Number: 9166017V FDA UDI
Primary DI / UDI-DI: 04022495252074 FDA UDI
FDA Product Code: FMF FDA UDI
GMDN Term: Metered-delivery hypodermic syringe FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Total Volume — 1.0 Milliliter FDA UDI

Category: Metered-delivery hypodermic syringe

Injekt® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: B. Braun Medical Inc.

Sources (1)

FDA UDI 91bdd96f-85e5-4054-8b48-52e42bbc5e2e 37 fields · synced Jun 1, 2026