← Back to catalogue

BD Nokor

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Nokor FDA UDI
Generic Name
Medication transfer needle, non-filtering/non-vented FDA UDI
Device Name
NEEDLE VENTED NOKOR 18X1 TW FDA UDI
Model / Reference
305214 FDA UDI
Description
NEEDLE VENTED NOKOR 18X1 TW FDA UDI

Identifiers

Catalog Number
305214 FDA UDI
Primary DI / UDI-DI
00382903052141 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Medication transfer needle, non-filtering/non-vented FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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
Length — 1 Inch FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: Medication transfer needle, non-filtering/non-vented

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

Similar devices

Also classified as Medication transfer needle, non-filtering/non-vented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 0d8efab1-82e2-435e-ba46-5e2c744db313 36 fields · synced Jun 8, 2026