Primary Device ID | 00850025525213 |
NIH Device Record Key | a63bcb5d-1efe-4524-ab4f-25df5e49c553 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SINC |
Version Model Number | SINC35090US |
Company DUNS | 962545294 |
Company Name | REFLOW MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850025525213 [Primary] |
DQY | Catheter, Percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-27 |
Device Publish Date | 2024-02-19 |
00850025525220 | SINC35135US |
00850025525213 | The SINC™ (Selective Interventional Navigation Catheter) Support Catheters are single lumen ca |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SINC 98193171 not registered Live/Pending |
ReFlow Medical, Inc. 2023-09-22 |
SINC 98093317 not registered Live/Pending |
Granite Creek Capital Partners, L.L.C. 2023-07-20 |
SINC 79293967 not registered Live/Pending |
Digital Surgery Limited 2020-04-16 |
SINC 79211480 5440626 Live/Registered |
Nuheara IP Pty Ltd 2017-04-10 |
SINC 75132566 2048011 Dead/Cancelled |
SEBASTIAN WORLDWIDE INC. 1996-07-11 |
SINC 73112371 1076044 Dead/Expired |
ZUMCHAK, JOSEPH 1977-01-13 |