Primary Device ID | 00850392006100 |
NIH Device Record Key | 95536089-0398-4aaf-8516-8dd1b7047233 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NuStat Flex |
Version Model Number | XR-0348 |
Company DUNS | 028807882 |
Company Name | BEEKEN BIOMEDICAL LLC |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850392006100 [Primary] |
GS1 | 10850392006107 [Package] Package: Shelf Pack [10 Units] In Commercial Distribution |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-12 |
Device Publish Date | 2023-05-04 |
10850392006169 - NuStat XR | 2024-02-28 |
00850392006100 - NuStat Flex | 2023-05-12NuStat Flex hemostatic wound dressing |
00850392006100 - NuStat Flex | 2023-05-12 NuStat Flex hemostatic wound dressing |
00850392006155 - NuStat | 2023-03-09 NuStat 4x4 |
00850392006018 - NuStat | 2022-11-28 |
00850392006179 - NuStat Trauma Pad XR | 2021-01-18 |
00850392006223 - NuStat Flex XR | 2021-01-18 |
00850392006230 - NuStat Flex XR | 2021-01-18 |
00850392006247 - NuStat Flex XR | 2021-01-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NUSTAT FLEX 86414484 4914732 Live/Registered |
Beeken Biomedical LLC 2014-10-03 |