← Back to catalogue

EXEL Huber Infusion Set

FDA UDI

Class II (US FDA UDI)

by Exel International

Identity

Trade Name
EXEL Huber Infusion Set FDA UDI
Generic Name
Vascular port administration set FDA UDI
Device Name
Huber Infusion Set, non-coring, right angle, 22G X 3/4, with Y injection site, rotating wing, 7"tube FDA UDI
Model / Reference
27949 FDA UDI
Description
Huber Infusion Set, non-coring, right angle, 22G X 3/4, with Y injection site, rotating wing, 7"tube FDA UDI

Identifiers

Catalog Number
27949 FDA UDI
Primary DI / UDI-DI
10020221279495 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Vascular port administration set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
Not 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

EXEL Huber Infusion Set by Exel International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 28cc919d-7ba9-4d67-94f6-cb46f0a2c6a0 35 fields · synced Jun 6, 2026