Catalog Number

185119

Brand Name

Ambler Surgical

Version/Model Number

Infusion cannula

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

-

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

HMX

Product Code Name

Cannula, ophthalmic

Public Device Record Key

c4b0f279-ec94-49c7-b070-40e0862175f6

Public Version Date

January 12, 2021

Public Version Number

1

DI Record Publish Date

January 04, 2021

Package DI Number

00190660199296

Quantity per Package

5

Contains DI Package

10190660199293

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BX