BA KIT,WE,P37,INL,1',BE,P37,INL,1',STKR - BA KIT,WE,P37,INL,1',BE,P37,INL,1',STKR - CURBELL MEDICAL PRODUCTS, INC.

Duns Number:796452311

Device Description: BA KIT,WE,P37,INL,1',BE,P37,INL,1',STKR

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More Product Details

Catalog Number

27892

Brand Name

BA KIT,WE,P37,INL,1',BE,P37,INL,1',STKR

Version/Model Number

300909910808

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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

-

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 Details

Product Code

ILQ

Product Code Name

System, Communication, Powered

Device Record Status

Public Device Record Key

2e45b069-2a2b-4c7b-918e-7f0ccb7cd126

Public Version Date

September 02, 2022

Public Version Number

1

DI Record Publish Date

August 25, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CURBELL MEDICAL PRODUCTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 478
2 A medical device with a moderate to high risk that requires special controls. 8062