| Primary Device ID | 00615233081810 |
| NIH Device Record Key | 5548f8f6-b9a0-4b0f-8ce1-801894b13efb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tissue-Tek® Quick-Ray™ |
| Version Model Number | 8018 |
| Catalog Number | 8018 |
| 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 | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00615233081810 [Primary] |
| KER | CONTAINER, EMBEDDING |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-03-25 |
| Device Publish Date | 2020-03-17 |
| 00615233081834 | Recipient Base Mold; 3/case |
| 00615233081827 | Recipient Block, 5 mm |
| 00615233081810 | Recipient Block, 3 mm |
| 00615233081803 | Recipient Block, 2 mm |
| 00615233081797 | Recipient Block, 1 mm |
| 00615233081735 | Tissue Microarray System |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TISSUE-TEK 72084436 0743380 Live/Registered |
LAB-TEK PLASTICS CO. 1959-11-02 |