Miser™ MISER5/C
GUDID 10884450109127
Merit Medical Systems, Inc.
Intravenous administration set| Primary Device ID | 10884450109127 |
| NIH Device Record Key | afc167c0-bc22-443a-adc6-51b3f5a7c6f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Miser™ |
| Version Model Number | 00884450109120 |
| Catalog Number | MISER5/C |
| 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 | 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 Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450109120 [Primary] |
| GS1 | 10884450109127 [Package] Contains: 00884450109120 Package: [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K083576
FDA Product Code
| FPA | Set, administration, intravascular |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [Miser™]
| 10884450116989 | 00884450116982 |
| 10884450109127 | 00884450109120 |
| 10884450099893 | 00884450099896 |
| 10884450014223 | 00884450014226 |
| 10884450014216 | 00884450014219 |
Trademark Results [Miser]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MISER 78073034 not registered Dead/Abandoned |
General Electric Company 2001-07-10 |
 MISER 76133436 2648186 Live/Registered |
AURUM TECHNOLOGY, LLC 2000-09-05 |
 MISER 75510862 2277875 Live/Registered |
FULLER INDUSTRIES, LLC 1998-06-30 |
 MISER 74587513 1923517 Live/Registered |
MERIT MEDICAL SYSTEMS, INC. 1994-10-19 |
 MISER 74447891 1985992 Dead/Cancelled |
Lynch, Jones & Ryan, Inc. 1993-10-18 |
 MISER 74177964 1701528 Dead/Cancelled |
MARATHON EQUIPMENT COMPANY 1991-06-20 |
 MISER 73808618 1581274 Dead/Cancelled |
BALLY MANUFACTURING CORPORATION 1989-06-23 |
 MISER 73603957 1424890 Dead/Cancelled |
FULLER BRUSH COMPANY, THE 1986-06-13 |
 MISER 73563914 1392277 Dead/Cancelled |
GENERAL ELECTRIC COMPANY 1985-10-18 |
 MISER 73563242 1407451 Dead/Cancelled |
MODULAR INFORMATION SYSTEMS, INC. 1985-10-15 |
 MISER 73510886 1345964 Dead/Cancelled |
HOME PRIDE MANUFACTURING, INC. 1984-11-28 |
 MISER 73407648 1269219 Dead/Cancelled |
Haas Door Company 1982-12-29 |
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