SCANLAN® In Situ Valvulotomes - Valvulotome - SCANLAN INTERNATIONAL INC

Duns Number:023055619

Device Description: Valvulotome

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More Product Details

Catalog Number

9009-125

Brand Name

SCANLAN® In Situ Valvulotomes

Version/Model Number

9009-125

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)

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

MGZ

Product Code Name

Valvulotome

Device Record Status

Public Device Record Key

87d19d7d-bd04-4890-b83c-f33c3e0c823f

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 02, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SCANLAN INTERNATIONAL INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1949
2 A medical device with a moderate to high risk that requires special controls. 855