Catalog Number

220493

Brand Name

ambIT

Version/Model Number

220493

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

OFQ

Product Code Name

Anesthesia Kit

Public Device Record Key

e378b5a1-fcbd-476e-baf0-c9fb81b1a7b6

Public Version Date

September 13, 2018

Public Version Number

3

DI Record Publish Date

September 09, 2016

Package DI Number

20857595005217

Quantity per Package

5

Contains DI Package

00857595005213

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-