IntraMarX - The IntraMarX capsule can be used for the - ANX ROBOTICA CORP

Duns Number:024972857

Device Description: The IntraMarX capsule can be used for the diagnosis of many GI conditions, including chron The IntraMarX capsule can be used for the diagnosis of many GI conditions, including chronic constipation, colonic inertia, hypomotility and outlet delay. Each of the IntraMarX capsules contains 24 tiny radiopaque rings within the capsule shell. The capsule is swallowed by the patient under the direction of physician. As this capsule moves through the digestive system, the capsule shell will dissolve and leave the rings in the GI tract of the patient; which will show up later during an X-ray scan. Five days after swallowing the capsule, a single scan of the abdomen will be taken to see the location of the rings and how many are left in the GI tract of the patient. The physician will make evaluations based on the rings remaining and make a diagnosis of GI conditions of the patient.

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More Product Details

Catalog Number

AGIROMC1-1-DD/1

Brand Name

IntraMarX

Version/Model Number

AGIROMC1-1-DD/1

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

K191087

Product Code Details

Product Code

FFX

Product Code Name

System, Gastrointestinal Motility (Electrical)

Device Record Status

Public Device Record Key

0ff351d8-4f8e-46bf-ad85-58aee8e30613

Public Version Date

July 16, 2020

Public Version Number

1

DI Record Publish Date

July 08, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ANX ROBOTICA CORP" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 10