HEPRO.US Syringe with 3ml/cc 22G x 3/4 - 100/Box

FDA UDI

Class II (US FDA UDI)

by Hepro.us Inc.

Identity

Trade Name: HEPRO.US Syringe with 3ml/cc 22G x 3/4 - 100/Box FDA UDI
Generic Name: General-purpose syringe, single-use FDA UDI
Device Name: Syringe with Attached Needle 3ml/cc 22G x 3/4 Box 100 units FDA UDI
Model / Reference: BX 3ml/cc 22G x 3/4 FDA UDI
Description: Syringe with Attached Needle 3ml/cc 22G x 3/4 Box 100 units FDA UDI

Identifiers

Primary DI / UDI-DI: 00854427007636 FDA UDI
FDA Product Code: FMF FDA UDI
GMDN Term: General-purpose syringe, single-use 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: General-purpose syringe, single-use

HEPRO.US Syringe with 3ml/cc 22G x 3/4 - 100/Box by Hepro.us Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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BD Safety-Lok — BECTON DICKINSON AND COMPANY · Class II
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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: Hepro.us Inc.

Sources (1)

FDA UDI 7443ec49-6390-4f70-ba54-b0c43e582fb5 33 fields · synced May 30, 2026