COMEG MEDICAL - This device is designed to create - SOPRO

Duns Number:264205501

Device Description: This device is designed to create pneumoperitoneum (distension of the abdomen with CO2 gas This device is designed to create pneumoperitoneum (distension of the abdomen with CO2 gas) as part of a diagnostic and/or operative laparoscopy procedure.

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More Product Details

Catalog Number

S_640_2008

Brand Name

COMEG MEDICAL

Version/Model Number

INSUFF SOPRO 20L PACK 1 EU

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

-

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

K070783

Product Code Details

Product Code

HIF

Product Code Name

Insufflator, Laparoscopic

Device Record Status

Public Device Record Key

961ff8f6-aa63-4e6f-b26e-fdb9df7568fe

Public Version Date

December 20, 2018

Public Version Number

1

DI Record Publish Date

November 19, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"SOPRO" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2
2 A medical device with a moderate to high risk that requires special controls. 128