Primary Device ID | 10884450007140 |
NIH Device Record Key | e01ad6af-de71-4ca0-8f2f-7b2e4b76c3ef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MBA™ |
Version Model Number | 00884450007143 |
Catalog Number | MAP403/B |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450007143 [Primary] |
GS1 | 10884450007140 [Package] Contains: 00884450007143 Package: [25 Units] In Commercial Distribution |
GS1 | 20884450007147 [Package] Package: [4 Units] In Commercial Distribution |
DTL | Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-03-05 |
Device Publish Date | 2016-09-24 |
10884450028558 | 00884450028551 |
10884450024437 | 00884450024430 |
20884450008540 | 00884450008546 |
10884450007140 | 00884450007143 |
10884450651121 | 00884450651124 |
20884450650701 | 00884450650707 |
10884450668747 | A |
20884450818101 | C |