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BD Veo

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Veo FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
BD Veo Insulin Syringes with BD Ultra-Fine Needle, U-100, 6mm, 31G, 0.3mL FDA UDI
Model / Reference
324931 FDA UDI
Description
BD Veo Insulin Syringes with BD Ultra-Fine Needle, U-100, 6mm, 31G, 0.3mL FDA UDI

Identifiers

Catalog Number
324931 FDA UDI
Primary DI / UDI-DI
30382903249313 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

Yes

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 — 0.3 Milliliter FDA UDI
Needle Gauge — 31 Gauge FDA UDI
Length — 6 Millimeter FDA UDI

Category: Insulin syringe/needle, basic

BD Veo 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 88fd454e-06cf-41d6-8d37-eb6ef951d455 36 fields · synced Jun 1, 2026