Super Sheath - TOGO MEDIKIT CO.,LTD.

Duns Number:690724240

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More Product Details

Catalog Number

-

Brand Name

Super Sheath

Version/Model Number

(16037-09B) BT90Z25TPW038

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

K141070,K141070

Product Code Details

Product Code

DYB

Product Code Name

INTRODUCER, CATHETER

Device Record Status

Public Device Record Key

3aa983e5-e759-4490-b931-027be337f7bd

Public Version Date

February 26, 2021

Public Version Number

7

DI Record Publish Date

September 16, 2016

Additional Identifiers

Package DI Number

14543527202418

Quantity per Package

1

Contains DI Package

04543527202411

Package Discontinue Date

December 11, 2020

Package Status

Not in Commercial Distribution

Package Type

Box

"TOGO MEDIKIT CO.,LTD." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 211