Primary Device ID | 00850015518133 |
NIH Device Record Key | 0ff351d8-4f8e-46bf-ad85-58aee8e30613 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IntraMarX |
Version Model Number | AGIROMC1-1-DD/1 |
Catalog Number | AGIROMC1-1-DD/1 |
Company DUNS | 024972857 |
Company Name | ANX ROBOTICA CORP |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850015518133 [Primary] |
FFX | System, Gastrointestinal Motility (Electrical) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-16 |
Device Publish Date | 2020-07-08 |
00850015518140 | The IntraMarX capsule can be used for the diagnosis of many GI conditions, including chronic con |
00850015518133 | The IntraMarX capsule can be used for the diagnosis of many GI conditions, including chronic con |
00850015518126 | The IntraMarX capsule can be used for the diagnosis of many GI conditions, including chronic con |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INTRAMARX 88945659 not registered Live/Pending |
ANKON MEDICAL TECHNOLOGIES (SHANGHAI) CO., LTD. 2020-06-03 |