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BD Integra

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Integra FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
NEEDLE INTEGRA 23X1 RB TW FDA UDI
Model / Reference
305312 FDA UDI
Description
NEEDLE INTEGRA 23X1 RB TW FDA UDI

Identifiers

Catalog Number
305312 FDA UDI
Primary DI / UDI-DI
00382903053124 FDA UDI
510(k) Number
K011103 FDA UDI
FDA Product Code
MEG FDA UDI
GMDN Term
Hypodermic needle, 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

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
Needle Gauge — 23 Gauge FDA UDI
Length — 1 Inch FDA UDI

Category: Hypodermic needle, single-use

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

Similar devices

Also classified as Hypodermic needle, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4bcf826b-a778-483f-8237-e153338fce3e 36 fields · synced May 30, 2026