Primary Device ID | 00615233081803 |
NIH Device Record Key | b9f6a471-5fd7-4497-904d-2f5f882a7e18 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tissue-Tek® Quick-Ray™ |
Version Model Number | 8017 |
Catalog Number | 8017 |
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 | 00615233081803 [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 |