Catalog Number

405912RC

Brand Name

TAUT

Version/Model Number

IPN006614

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

K010007,K010007,K010007

Product Code

GCJ

Product Code Name

Laparoscope, general & plastic surgery

Public Device Record Key

8af8c9b5-9c55-4807-8a71-98b92a2e6ae9

Public Version Date

November 06, 2020

Public Version Number

8

DI Record Publish Date

September 16, 2016

Package DI Number

44026704505126

Quantity per Package

4

Contains DI Package

24026704505122

Package Discontinue Date

June 26, 2020

Package Status

Not in Commercial Distribution

Package Type

Box