Primary Device ID | 00615233078797 |
NIH Device Record Key | dd8579a8-3b48-46f1-8956-25c5c6d48f7c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tissue-Tek Film® |
Version Model Number | 4740 |
Catalog Number | 4740 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00615233078797 [Primary] |
KIM | DEVICE FOR SEALING MICROSECTIONS |
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 |
00615233078827 | Coverslipper with Barcode Reader |
00615233078797 | Coverslipper |
04946433600478 | Coverslipper |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TISSUE-TEK FILM 78503251 3248204 Live/Registered |
Sakura Finetek U.S.A., Inc. 2004-10-20 |