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BD Insulin Syringe

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Insulin Syringe FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
U-100 Insulin Syringe, 1.0mL, 27G x 12.7mm FDA UDI
Model / Reference
324705 FDA UDI
Description
U-100 Insulin Syringe, 1.0mL, 27G x 12.7mm FDA UDI

Identifiers

Catalog Number
324705 FDA UDI
Primary DI / UDI-DI
10382903247056 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 12.7 Millimeter FDA UDI
Needle Gauge — 27 Gauge FDA UDI
Total Volume — 1.0 Milliliter FDA UDI

Category: Insulin syringe/needle, basic

BD Insulin Syringe by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin syringe/needle, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e94b9267-10b5-4b4f-a446-49f52f6c571d 35 fields · synced May 30, 2026