HEPRO.US 0.3ml/cc 29G x 5/16"

FDA UDI

Class II (US FDA UDI)

by Hepro.us Inc.

Identity

Trade Name: HEPRO.US 0.3ml/cc 29G x 5/16" FDA UDI
Generic Name: Insulin syringe/needle, basic FDA UDI
Device Name: HEPRO.US Insulin Syringes attached needle 0.3ml/cc 29Gx 5/16" Box 100 FDA UDI
Model / Reference: BX 0.3ml/cc 29G x 5/16" FDA UDI
Description: HEPRO.US Insulin Syringes attached needle 0.3ml/cc 29Gx 5/16" Box 100 FDA UDI

Identifiers

Primary DI / UDI-DI: 00850578007464 FDA UDI
FDA Product Code: FMF FDA UDI
GMDN Term: Insulin syringe/needle, basic 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: Insulin syringe/needle, basic

HEPRO.US 0.3ml/cc 29G x 5/16" by Hepro.us Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Ultra-Care Insulin Syringe 30G 5/16" 0.5 CC 100 Ct — ARISE MEDICAL LLC · Class II

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 b1861b0f-f4b9-4acc-92db-bb471cff4862 33 fields · synced May 30, 2026