E-Cath Plus acc. Tsui - E-Cath Plus acc. Tsui SonoPlex - Pajunk GmbH Medizintechnologie

Duns Number:317654283

Device Description: E-Cath Plus acc. Tsui SonoPlex Stim cannula 21G x 101mm indwelling E-Cath Plus acc. Tsui SonoPlex Stim cannula 21G x 101mm indwelling catheter 18G x 83mm

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More Product Details

Catalog Number

241185-41E

Brand Name

E-Cath Plus acc. Tsui

Version/Model Number

241185-41E

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 31, 2019

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Unsafe

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

K152952,K152952

Product Code Details

Product Code

BSO

Product Code Name

CATHETER, CONDUCTION, ANESTHETIC

Device Record Status

Public Device Record Key

344fdfa5-8358-4ec0-9528-26485f221709

Public Version Date

December 31, 2019

Public Version Number

6

DI Record Publish Date

October 14, 2016

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