Luer Loc Standard Syringe

FDA UDI

Class II (US FDA UDI)

by Remington Medical, Inc.

Identity

Trade Name: Luer Loc Standard Syringe FDA UDI
Generic Name: General-purpose syringe, single-use FDA UDI
Device Name: 10cc (Yellow) FDA UDI
Model / Reference: LLS-10-Y FDA UDI
Description: 10cc (Yellow) FDA UDI

Identifiers

Catalog Number: LLS-10-Y FDA UDI
Primary DI / UDI-DI: 00813079020097 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

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

Sterilization Method

Ethylene Oxide FDA UDI

Dimensions & Sizes

Size: Total Volume — 10 Milliliter FDA UDI

Category: General-purpose syringe, single-use

Luer Loc Standard Syringe by Remington 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: Remington Medical, Inc.

Sources (1)

FDA UDI c7b4ae82-2a9b-4518-b82a-413c1c58858d 36 fields · synced Jun 8, 2026