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BD SafetyGlide

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD SafetyGlide FDA UDI
Generic Name
General-purpose syringe/needle FDA UDI
Device Name
SYRINGE 5ML LL W/NDL SFTYGLD 22X1-1/2 RB FDA UDI
Model / Reference
305907 FDA UDI
Description
SYRINGE 5ML LL W/NDL SFTYGLD 22X1-1/2 RB FDA UDI

Identifiers

Catalog Number
305907 FDA UDI
Primary DI / UDI-DI
00382903059072 FDA UDI
FDA Product Code
MEG FDA UDI
GMDN Term
General-purpose syringe/needle 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI
Needle Gauge — 22 Gauge FDA UDI
Length — 1.5 Inch FDA UDI

Category: General-purpose syringe/needle

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/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI baf87536-8ea3-4116-bc2f-f39b4e8f085a 36 fields · synced May 31, 2026