Primary Device ID | 10884450160487 |
NIH Device Record Key | 6b57dd2b-3000-4f1e-892b-fb97516c401e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PhD™ |
Version Model Number | 00884450160480 |
Catalog Number | MAP800 |
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 | 00884450160480 [Primary] |
GS1 | 10884450160487 [Package] Contains: 00884450160480 Package: [25 Units] In Commercial Distribution |
GS1 | 20884450160484 [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 | 2 |
Public Version Date | 2020-03-05 |
Device Publish Date | 2019-05-24 |
10884450160487 | 00884450160480 |
20884450160507 | 00884450160503 |
10884450292751 | 00884450292754 |
20884450160491 | 00884450160497 |
10884450160517 | 00884450160510 |
20884450292789 | 00884450292785 |
10884450291969 | 00884450291962 |
10884450160524 | 00884450160527 |
10884450292775 | 00884450292778 |
20884450746725 | 00884450746721 |
10884450746742 | 00884450746745 |
10884450746827 | 00884450746820 |
20884450746718 | 00884450746714 |
10884450746766 | 00884450746769 |
20884450746817 | 00884450746813 |
10884450746780 | B |
10884450003982 | T |