Primary Device ID | 00615233082367 |
NIH Device Record Key | b77dca77-841f-433d-8166-7a20b58242b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VisionTek® |
Version Model Number | 9011 |
Catalog Number | 9011 |
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 | true |
Serial Number | false |
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 | 00615233082367 [Primary] |
IBJ | LIGHT, MICROSCOPE |
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 |
00615233082268 | Digital Microscope |
00615233082367 | Slide Carrier |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VISIONTEK 88629110 not registered Live/Pending |
VisionTek Products, LLC 2019-09-24 |
VISIONTEK 87070811 not registered Dead/Abandoned |
Shenzhen Visiontek Electronic Technology Co., Limited 2016-06-14 |
VISIONTEK 85399322 4455471 Live/Registered |
Sakura Finetek, U.S.A., Inc. 2011-08-16 |
VISIONTEK 74696957 2045429 Live/Registered |
VISIONTEK PRODUCTS, LLC. 1995-07-03 |
VISIONTEK 74516806 2095471 Dead/Cancelled |
VISIONTEK, INC. 1994-04-25 |