Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Medline FDA UDI
Generic Name: Metered-delivery hypodermic syringe/needle FDA UDI
Device Name: NEEDLE,HYPODERM,SAFETY, 25GX1.5 FDA UDI
Model / Reference: SSN100257 FDA UDI
Description: NEEDLE,HYPODERM,SAFETY, 25GX1.5 FDA UDI

Identifiers

Catalog Number: SSN100257 FDA UDI
Primary DI / UDI-DI: 10193489031997 FDA UDI
FDA Product Code: FMF FDA UDI
MEG FDA UDI
FMI FDA UDI
GMDN Term: Metered-delivery hypodermic syringe/needle FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 FDA UDI
880.5570 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

Category: Metered-delivery hypodermic syringe/needle

Medline by Medline Industries, 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: Medline Industries, Inc.

Sources (1)

FDA UDI c1ffbf90-0099-403c-a830-5bffc0f12768 35 fields · synced May 29, 2026