Smart Tip™ ST800
GUDID 10884450007669
Merit Medical Systems, Inc.
General-purpose syringe, single-use| Primary Device ID | 10884450007669 |
| NIH Device Record Key | 0ebd5c20-958e-45b0-b9e6-4fc5ba05d136 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Smart Tip™ |
| Version Model Number | 00884450007662 |
| Catalog Number | ST800 |
| 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 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 | 00884450007662 [Primary] |
| GS1 | 10884450007669 [Package] Contains: 00884450007662 Package: [25 Units] In Commercial Distribution |
| GS1 | 20884450007666 [Package] Package: [4 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K875196
FDA Product Code
| FMF | Syringe, piston |
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 | 2018-09-12 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [Smart Tip™]
| 20884450075603 | 00884450075609 |
| 20884450055421 | 00884450055427 |
| 20884450007710 | 00884450007716 |
| 20884450007703 | 00884450007709 |
| 10884450007690 | 00884450007693 |
| 10884450007683 | 00884450007686 |
| 20884450007673 | 00884450007679 |
| 10884450007669 | 00884450007662 |
| 10884450610616 | A |
| 10884450610630 | A |
| 10884450610555 | A |
| 10884450610579 | A |
| 10884450610593 | A |
Trademark Results [Smart Tip]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SMART TIP 86867529 not registered Dead/Abandoned |
Activator Methods International, Ltd. 2016-01-06 |
 SMART TIP 76634988 3767749 Dead/Cancelled |
Diamond Billiard Products, Inc. 2005-04-04 |
 SMART TIP 76157115 not registered Dead/Abandoned |
Federal Marketing Corp. 2000-10-31 |
 SMART TIP 73325288 1243824 Dead/Cancelled |
Teledyne Industries, Inc. 1981-08-26 |
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