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BD QUINCKE Spinal Needles

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD QUINCKE Spinal Needles FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
NEEDLE SPINAL S/SU 22GA 3-1/2IN QUINCKE FDA UDI
Model / Reference
405181 FDA UDI
Description
NEEDLE SPINAL S/SU 22GA 3-1/2IN QUINCKE FDA UDI

Identifiers

Catalog Number
405181 FDA UDI
Primary DI / UDI-DI
00382904051815 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 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 — 3.5 Inch FDA UDI

Category: Spinal needle, single-useEvacuated blood collection tube IVD, anticoagulant/antiglycolytic

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

Similar devices

Also classified as Evacuated blood collection tube IVD, anticoagulant/antiglycolytic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI f485e0bd-2df2-476a-90c0-42ba317841c6 36 fields · synced Jun 6, 2026