Catalog Number

-

Brand Name

Resp-O2 Disposable Suction Liners, 3000cc

Version/Model Number

32262

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KDQ

Product Code Name

Bottle, Collection, Vacuum

Public Device Record Key

6b2bc121-5fbd-4886-9f9e-79035dfa7a7e

Public Version Date

May 17, 2022

Public Version Number

1

DI Record Publish Date

May 09, 2022

Package DI Number

00840117321540

Quantity per Package

50

Contains DI Package

00840117321601

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case