Primary Device ID | 10884450332389 |
NIH Device Record Key | 2819de23-da68-418c-8e95-ec7b6dd3bd1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ArgoTrans™ |
Version Model Number | 10884450332389 |
Catalog Number | 041596505A/A |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 20 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | 00884450332382 [Unit of Use] |
GS1 | 10884450332389 [Primary] |
DRS | Transducer, blood-pressure, extravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-10-11 |
Device Publish Date | 2019-09-03 |
10884450332815 | 10884450332815 |
10884450332419 | 10884450332419 |
10884450332372 | 10884450332372 |
10884450332488 | 10884450332488 |
00884450332825 | 10884450332822 |
10884450332839 | 10884450332839 |
10884450332549 | 10884450332549 |
10884450332532 | 10884450332532 |
10884450332525 | 10884450332525 |
10884450332518 | 10884450332518 |
10884450332501 | 10884450332501 |
10884450332495 | 10884450332495 |
10884450332433 | 10884450332433 |
10884450332426 | 10884450332426 |
10884450332389 | 10884450332389 |
10884450332341 | 10884450332341 |
00884450332801 | 10884450332808 |