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EXEL Spinal Needle

FDA UDI

Class II (US FDA UDI)

by Exel International

Identity

Trade Name
EXEL Spinal Needle FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
Spinal Needle, 22G x 2 3/4, QUINCKE BEVEL FDA UDI
Model / Reference
26965 FDA UDI
Description
Spinal Needle, 22G x 2 3/4, QUINCKE BEVEL FDA UDI

Identifiers

Catalog Number
26965 FDA UDI
Primary DI / UDI-DI
10020221269656 FDA UDI
510(k) Number
K895771 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

Category: Spinal needle, single-use

EXEL Spinal Needle by Exel International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal needle, single-use.

Cleared under the same submission

K895771 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Exel International

Sources (1)

  • FDA UDI ab602d38-4720-4ee3-93e6-7e93cea80e45 35 fields · synced May 29, 2026