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Universal Funnel Adapter

FDA UDI

Class I (US FDA UDI)

by Uresil Corp.

Identity

Trade Name
Universal Funnel Adapter FDA UDI
Generic Name
Luer/non-ISO80369-standardized linear connector, single-use FDA UDI
Device Name
Universal Funnel Adapter-Luer Lock FDA UDI
Model / Reference
UFA-LL FDA UDI
Description
Universal Funnel Adapter-Luer Lock FDA UDI

Identifiers

Catalog Number
UFA-LL FDA UDI
Primary DI / UDI-DI
H862UFALL0 FDA UDI
FDA Product Code
GBO FDA UDI
GMDN Term
Luer/non-ISO80369-standardized linear connector, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer/non-ISO80369-standardized linear connector, single-use

Universal Funnel Adapter by Uresil Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer/non-ISO80369-standardized linear connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uresil Corp.

Sources (1)

  • FDA UDI f7871843-0206-4d5b-9555-1be1ae3ff10c 36 fields · synced May 30, 2026