Primary Device ID | 00850011790052 |
NIH Device Record Key | 44714b7a-a6d4-4c0e-8990-18eb1bc572a9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flex Passive Driver Kit- Small |
Version Model Number | REFPDS19 |
Company DUNS | 036969003 |
Company Name | RESOUNDANT, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850011790052 [Primary] |
LNH | System, Nuclear Magnetic Resonance Imaging |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-10 |
Device Publish Date | 2023-04-01 |
00850011790045 - Flex Passive Driver Kit- Large | 2023-04-10 |
00850011790052 - Flex Passive Driver Kit- Small | 2023-04-10 |
00850011790052 - Flex Passive Driver Kit- Small | 2023-04-10 |
00850011790106 - Passive Driver | 2023-03-01 |
00850011790199 - Hepatogram Plus | 2022-04-21 |
00850011790007 - MREplus | 2021-04-09 |
00850011790014 - MREplus | 2021-04-09 |