Primary Device ID | 20884450024403 |
NIH Device Record Key | 73345f58-2f08-4b3d-8de0-a1b8a2cbfeb7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Merit Disposal Depot™ |
Version Model Number | 00884450024409 |
Catalog Number | K10-01103 |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00884450024409 [Primary] |
GS1 | 10884450024406 [Package] Contains: 00884450024409 Package: [10 Units] In Commercial Distribution |
GS1 | 20884450024403 [Package] Contains: 10884450024406 Package: [4 Units] In Commercial Distribution |
PPD | Universal drainage tray |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-15 |
Device Publish Date | 2018-09-13 |
10884450123130 | 00884450123133 |
20884450050105 | 00884450050101 |
20884450028579 | 00884450028575 |
10884450024451 | 00884450024454 |
20884450024403 | 00884450024409 |
10884450023676 | 00884450023679 |
20884450022850 | 00884450022856 |
20884450022089 | 00884450022085 |
20884450019607 | 00884450019603 |
20884450013421 | 00884450013427 |
20884450008236 | 00884450008232 |
20884450008229 | 00884450008225 |
10884450419769 | 00884450419762 |
20884450504936 | 00884450504932 |
10884450790714 | Initial Release |