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EXEL Comfort Point Insulin Syringe

FDA UDI

Class II (US FDA UDI)

by Exel International

Identity

Trade Name
EXEL Comfort Point Insulin Syringe FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
Insulin Syringe, 0.5cc, 28G X 1/2 FDA UDI
Model / Reference
26026 FDA UDI
Description
Insulin Syringe, 0.5cc, 28G X 1/2 FDA UDI

Identifiers

Catalog Number
26026 FDA UDI
Primary DI / UDI-DI
20020221260261 FDA UDI
510(k) Number
K861153 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Insulin syringe/needle, basic 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

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: Insulin syringe/needle, basic

EXEL Comfort Point Insulin Syringe by Exel International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin syringe/needle, basic.

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 7bd476e9-95a1-4247-ace5-7a27cf5b0f42 35 fields · synced May 30, 2026