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Exel Hypo Ndl 16 X3/4" Bulk, N-S

FDA UDI

Class II (US FDA UDI)

by Exel International

Identity

Trade Name
EXEL HYPO NDL 16 X3/4" BULK, N-S FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
EXEL HYPO NDL 16 X3/4" BULK, N-S 20,000/CTN FDA UDI
Model / Reference
26423BN FDA UDI
Description
EXEL HYPO NDL 16 X3/4" BULK, N-S 20,000/CTN FDA UDI

Identifiers

Catalog Number
26423BN FDA UDI
Primary DI / UDI-DI
00020221664232 FDA UDI
510(k) Number
K861153 FDA UDI
FDA Product Code
FMF 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Hypodermic needle, single-use

Exel Hypo Ndl 16 X3/4" Bulk, N-S by Exel International — 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

Manufacturer
Exel International

Sources (1)

  • FDA UDI c6aa8717-b057-437d-8b44-6b0fbd6751d6 36 fields · synced May 30, 2026