Endoclinch grasp.fcps.,fenestr.,d/a, 5/330mm - Endoclinch grasp.fcps.,fenestr.,d/a, 5/330mm - mahe medical gmbh

Duns Number:342243334

Device Description: Endoclinch grasp.fcps.,fenestr.,d/a, 5/330mm

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More Product Details

Catalog Number

22.054.33

Brand Name

Endoclinch grasp.fcps.,fenestr.,d/a, 5/330mm

Version/Model Number

22.054.33

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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"

Yes

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

GCJ

Product Code Name

Laparoscope, general & plastic surgery

Device Record Status

Public Device Record Key

a2f0de27-b221-43bf-9bb2-44be550b56b0

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 03, 2016

Additional Identifiers

Package DI Number

EMAH22054331

Quantity per Package

1

Contains DI Package

EMAH22054330

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"MAHE MEDICAL GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 19
2 A medical device with a moderate to high risk that requires special controls. 1976