Catalog Number

1D5050

Brand Name

LMA AIRWAY MANAGEMENT

Version/Model Number

IPN047908

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

CAE

Product Code Name

AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

Public Device Record Key

5248e12d-1cc3-4b2b-b9df-1e0c13ce2028

Public Version Date

February 22, 2021

Public Version Number

3

DI Record Publish Date

September 15, 2018

Package DI Number

15060112313957

Quantity per Package

10

Contains DI Package

05060112313950

Package Discontinue Date

February 19, 2021

Package Status

Not in Commercial Distribution

Package Type

Box