NRG Transseptal Needle - Baylis Médicale Cie Inc

Duns Number:249225954

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More Product Details

Catalog Number

-

Brand Name

NRG Transseptal Needle

Version/Model Number

NRG-98-C1

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

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 Details

Product Code

DXF

Product Code Name

Catheter, Septostomy

Device Record Status

Public Device Record Key

6b210207-8d6e-4594-9371-bdb7dd88d21f

Public Version Date

March 25, 2022

Public Version Number

4

DI Record Publish Date

August 15, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BAYLIS MÉDICALE CIE INC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 1139