Primary Device ID | 00852184003083 |
NIH Device Record Key | ffba2270-c43b-41a9-bc8a-d0683304dd1c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeuRx DPS™ Surgical Site Start-up Kit |
Version Model Number | 20-0039 |
Company DUNS | 138432070 |
Company Name | Synapse Biomedical, 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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852184003083 [Primary] |
OIR | Diaphragmatic/Phrenic Nerve Laparoscopically-Implanted Stimulator |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2014-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEURX DPS 77422640 3726169 Live/Registered |
Synapse Biomedical, Inc. 2008-03-14 |