Primary Device ID | 10884450013295 |
NIH Device Record Key | 9265bb84-4558-4d1c-beef-1a2803e5b2d6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Merit S-MAK™ |
Version Model Number | 00884450013298 |
Catalog Number | S-MAK5F-15/A |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
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 | 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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450013298 [Primary] |
GS1 | 10884450013295 [Package] Contains: 00884450013298 Package: [5 Units] In Commercial Distribution |
GS1 | 20884450013292 [Package] Package: [15 Units] In Commercial Distribution |
DRE | DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
10884450155070 | 00884450155073 |
10884450155063 | 00884450155066 |
10884450155049 | 00884450155042 |
10884450144463 | 00884450144466 |
10884450144456 | 00884450144459 |
10884450144449 | 00884450144442 |
10884450144432 | 00884450144435 |
10884450013295 | 00884450013298 |
10884450013288 | 00884450013281 |
10884450013271 | 00884450013274 |
10884450012861 | 00884450012864 |
10884450012663 | 00884450012666 |
10884450012656 | 00884450012659 |
10884450012649 | 00884450012642 |
10884450012632 | 00884450012635 |
10884450012625 | 00884450012628 |
10884450012618 | 00884450012611 |
10884450410438 | 00884450410431 |