Tru-Cut® 2N2713X/B
GUDID 20884450443075
Merit Medical Systems, Inc.
Soft-tissue biopsy procedure kit, non-medicated| Primary Device ID | 20884450443075 |
| NIH Device Record Key | 020ffe48-2292-436c-b66c-f59a3d6d9561 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tru-Cut® |
| Version Model Number | 10884450443078 |
| Catalog Number | 2N2713X/B |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| Device Count | 10 |
| 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 | 00884450443071 [Unit of Use] |
| GS1 | 10884450443078 [Primary] |
| GS1 | 20884450443075 [Package] Contains: 10884450443078 Package: [2 Units] In Commercial Distribution |
FDA Product Code
| KNW | INSTRUMENT, BIOPSY |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-07 |
| Device Publish Date | 2022-09-29 |
On-Brand Devices [Tru-Cut®]
| 20884450443020 | 10884450443023 |
| 20884450443044 | 10884450443047 |
| 20884450443013 | 10884450443016 |
| 20884450394650 | 10884450394653 |
| 20884450394643 | 10884450394646 |
| 20884450443075 | 10884450443078 |
| 20884450394681 | 10884450394684 |
| 20884450443068 | 10884450443061 |
| 20884450831520 | C |
| 20884450831513 | C |
Trademark Results [Tru-Cut]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TRU-CUT 78654211 3313746 Live/Registered |
TECHNI AUTOMATION PTY LTD 2005-06-20 |
 TRU-CUT 76343538 not registered Dead/Abandoned |
MTD Products Inc 2001-11-30 |
 TRU-CUT 75829363 2495524 Dead/Cancelled |
TRUCUT INCORPORATED 1999-10-25 |
 TRU-CUT 75186481 2148865 Live/Registered |
MERIT MEDICAL SYSTEMS, INC. 1996-09-25 |
 TRU-CUT 74337241 not registered Dead/Abandoned |
TRU-CUT, INC. 1992-12-07 |
 TRU-CUT 74198093 1715043 Dead/Cancelled |
Continental Manufacturing & Supply, Ltd. 1991-08-26 |
 TRU-CUT 73697603 1598142 Dead/Cancelled |
GANEAUX INDUSTRIES, INC. 1987-11-25 |
 TRU-CUT 73330645 not registered Dead/Abandoned |
ABC TOOL INC. 1981-10-02 |
 TRU-CUT 73121701 1078352 Dead/Cancelled |
IMC Chemical Group, Inc. 1977-04-06 |
 TRU-CUT 73077527 1046748 Dead/Cancelled |
Baxter Laboratories, Inc. 0000-00-00 |
 TRU-CUT 73069224 1056466 Dead/Expired |
MILWAUKEE MOTIVE MFG. CO. 1975-11-17 |
 TRU-CUT 72303657 0891802 Dead/Expired |
BAXTER LABORATORIES, INC. 1968-07-26 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.