DiLumen C2 - DiLumen C2 consists of a soft flexible sheath - LUMENDI LLC

Duns Number:859290897

Device Description: DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The devi DiLumen C2 consists of a soft flexible sheath that fits over standard endoscopes. The device employs two balloons, one behind the bending section of the endoscope and the second in front of the tip of the endoscope. When both balloons are deployed, and inflated the area in between is stabilized. This Therapeutic Zone (TZ) facilitates stabilization, insufflation and manipulation of the tissue thus allowing the clinician to effectively treat the target area. The device also has two flexible tool channels attached on the outside of the sleeve at the 3 and 6 o'clock positions. These tool channels accommodate flexible endoscopic instruments used to perform endoscopic interventions. This DiLumen C2 version is designed to be used with the DiLumen Elbow Ig grasper.

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More Product Details

Catalog Number

D-2005

Brand Name

DiLumen C2

Version/Model Number

DiLumen C2.2 103 cm

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

K173317,K173317

Product Code Details

Product Code

FDF

Product Code Name

Colonoscope And Accessories, Flexible/Rigid

Device Record Status

Public Device Record Key

c9436525-2855-4689-b373-7a778c95d3ed

Public Version Date

January 03, 2020

Public Version Number

1

DI Record Publish Date

December 26, 2019

Additional Identifiers

Package DI Number

10858836007086

Quantity per Package

5

Contains DI Package

00858836007089

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"LUMENDI LLC" 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. 11