BD Luer-Lok, BD SafetyGlide

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name: BD Luer-Lok, BD SafetyGlide FDA UDI
Generic Name: General-purpose syringe, single-use FDA UDI
Device Name: SYRINGE 3ML LL W/NDL SFTYGLD 25X1 RB FDA UDI
Model / Reference: 305924 FDA UDI
Description: SYRINGE 3ML LL W/NDL SFTYGLD 25X1 RB FDA UDI

Identifiers

Catalog Number: 305924 FDA UDI
Primary DI / UDI-DI: 00382903059249 FDA UDI
FDA Product Code: MEG 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

Dimensions & Sizes

Size: Length — 1 Inch FDA UDI
Total Volume — 3 Milliliter FDA UDI

Category: General-purpose syringe, single-use

BD Luer-Lok, BD SafetyGlide by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

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SURGYCO — Surgyco LLC · Class I
NAMIC — MEDLINE INDUSTRIES, INC. · Class II
HSW HENKE-JECT® — Henke-Sass, Wolf GmbH · Class II
SURGYCO — Surgyco LLC · Class I
Merit Medical® — Merit Medical Systems, Inc. · 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: Becton Dickinson And Company

Sources (1)

FDA UDI 90512c3c-072c-497e-b4a8-4b0966c3b12f 36 fields · synced May 30, 2026