E-CATH TSUI - 251185-40E - Pajunk GmbH Medizintechnologie

Duns Number:317654283

Device Description: 251185-40E

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More Product Details

Catalog Number

251185-40E

Brand Name

E-CATH TSUI

Version/Model Number

251185-40E

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K152952,K152952,K152952

Product Code Details

Product Code

BSO

Product Code Name

CATHETER, CONDUCTION, ANESTHETIC

Device Record Status

Public Device Record Key

a8b8a3f2-1e68-45ad-8237-9ba7c1b7b000

Public Version Date

April 12, 2021

Public Version Number

1

DI Record Publish Date

April 02, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PAJUNK GMBH MEDIZINTECHNOLOGIE" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 35
2 A medical device with a moderate to high risk that requires special controls. 979