Catalog Number

UFA-LL

Brand Name

Universal Funnel Adapter

Version/Model Number

UFA-LL

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

April 30, 2026

Issuing Agency

In HIBCC

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GBO

Product Code Name

Catheter, Nephrostomy, General & Plastic Surgery

Public Device Record Key

f7871843-0206-4d5b-9555-1be1ae3ff10c

Public Version Date

April 15, 2022

Public Version Number

5

DI Record Publish Date

August 30, 2016

Package DI Number

H862UFALL2

Quantity per Package

50

Contains DI Package

H862UFALL0

Package Discontinue Date

April 30, 2026

Package Status

In Commercial Distribution

Package Type

Shipper