← Back to catalogue

Exel Hypo Ndl 20gx1" Bulk, N-S

FDA UDI

Class II (US FDA UDI)

by Exel International

Identity

Trade Name
EXEL HYPO NDL 20GX1" BULK, N-S FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
EXEL HYPO NDL 20GX1" BULK, N-S, 2bagsx10,000 20,000/CRTN FDA UDI
Model / Reference
26417BN FDA UDI
Description
EXEL HYPO NDL 20GX1" BULK, N-S, 2bagsx10,000 20,000/CRTN FDA UDI

Identifiers

Catalog Number
26417BN FDA UDI
Primary DI / UDI-DI
00020221664171 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 20gx1" 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

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

Manufacturer

Manufacturer
Exel International

Sources (1)

  • FDA UDI 4a06e6bf-e454-4f10-af48-ab4be5a3f0e9 36 fields · synced Jun 8, 2026