FDA UDI In Commercial Distribution 🇺🇸 United States

IntraMarX

DI: 00850015518140 · Model: AGIROMC-1-TC/1 · ANX ROBOTICA CORP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IntraMarX
Primary DI
00850015518140
Version / Model
AGIROMC-1-TC/1
Catalog Number
AGIROMC-1-TC/1
Company Name
ANX ROBOTICA CORP
Labeler DUNS
024972857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-08
Public Version
2
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
59ee1a93-0761-44c9-addc-5da0bb19392c

Device Description

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.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FFX System, Gastrointestinal Motility (Electrical)

GMDN Terms

Code Name
62385 Gastrointestinal telemetric monitoring system capsule, ingestible

Identifiers

Type ID
Primary 00850015518140

Premarket Submissions

Submission Number Supplement Number
K191087 000