BD® Quincke Spinal Needle

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name: BD® Quincke Spinal Needle FDA UDI
Generic Name: Spinal needle, single-use FDA UDI
Device Name: NEEDLE SPINAL S/SU 20GA 2-1/2IN QUINCKE FDA UDI
Model / Reference: 405071 FDA UDI
Description: NEEDLE SPINAL S/SU 20GA 2-1/2IN QUINCKE FDA UDI

Identifiers

Catalog Number: 405071 FDA UDI
Primary DI / UDI-DI: 00382904050719 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 20 Gauge FDA UDI
Length — 2.5 Inch FDA UDI

Category: Spinal needle, single-use

BD® Quincke Spinal Needle by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Becton Dickinson And Company

Sources (1)

FDA UDI 9dd4a4aa-4d58-4285-b00f-f57c610ce2ae 36 fields · synced Jun 1, 2026