Merit Advance®
GUDID 10884450018184
Merit Medical Systems, Inc.
Anaesthesia conduction catheter holder, sterile| Primary Device ID | 10884450018184 |
| NIH Device Record Key | 09ae736a-f91b-493f-ba77-2ebe048b0684 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Merit Advance® |
| Version Model Number | 00884450018187 |
| 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 Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450018187 [Primary] |
| GS1 | 10884450018184 [Package] Contains: 00884450018187 Package: [25 Units] In Commercial Distribution |
| GS1 | 20884450018181 [Package] Package: [4 Units] In Commercial Distribution |
FDA Product Code
| DRC | Trocar |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [Merit Advance®]
Trademark Results [Merit Advance]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MERIT ADVANCE 78924473 3314740 Live/Registered |
Merit Medical Systems, Inc. 2006-07-07 |
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