| Primary Device ID | 00615233008220 | 
| NIH Device Record Key | 9b0207da-fc4f-42d4-8397-fb60bbda4e4c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Accu-Cut® SRM™ 300 LT | 
| Version Model Number | 1300N | 
| Catalog Number | 1300N | 
| Company DUNS | 179135769 | 
| Company Name | SAKURA FINETEK U.S.A., INC. | 
| Device Count | 1 | 
| DM Exempt | true | 
| 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 | false | 
| Lot Batch | false | 
| Serial Number | true | 
| Manufacturing Date | true | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | false | 
| OTC Over-The-Counter | false | 
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | |
| Phone | +1(310)972-7800 | 
| TS@sakuraus.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00615233008220 [Primary] | 
| IDO | MICROTOME, ROTARY | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-02-14 | 
| Device Publish Date | 2020-02-06 | 
| 00615233008220 | Manual Microtome (Non-Retracting) | 
| 00615233008213 | Manual Microtome, Retracting | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  ACCU-CUT  77096552  3316453 Dead/Cancelled | Winsource Industries LTD. 2007-02-01 | 
|  ACCU-CUT  76503925  2873678 Live/Registered | Accu-Cut Diamond Bore sizing Systems, Inc. 2003-04-04 | 
|  ACCU-CUT  76503925  2873678 Live/Registered | Accu-Cut Diamond Tool Company, Inc. 2003-04-04 | 
|  ACCU-CUT  76323994  3250089 Live/Registered | Brockie International, Inc. 2001-10-12 | 
|  ACCU-CUT  76013931  2568218 Live/Registered | BIOPRO, INC. 2000-03-30 | 
|  ACCU-CUT  76005051  2959992 Live/Registered | STANLEY BLACK & DECKER, INC. 2000-03-20 | 
|  ACCU-CUT  76004328  not registered Dead/Abandoned | Brockie International, Inc. 2000-03-20 | 
|  ACCU-CUT  75626349  not registered Dead/Abandoned | EBI Medical Systems, Inc. 1999-01-19 | 
|  ACCU-CUT  75560579  not registered Dead/Abandoned | Brockie International, Inc 1998-09-28 | 
|  ACCU-CUT  75449654  2379912 Dead/Cancelled | SUFIX USA, INC. 1998-03-13 | 
|  ACCU-CUT  75089151  not registered Dead/Abandoned | Accu-Cut Diamond Tool Co., Inc. 1996-04-05 | 
|  ACCU-CUT  74508646  not registered Dead/Abandoned | McKeegan Equipment & Supply 1994-04-04 |