Primary Device ID | 00862095000491 |
NIH Device Record Key | 2b87e1ee-ca9e-406b-83f9-bc033b4d1299 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PeriWatch Vigilance Tracings |
Version Model Number | 2019 Rev 1.02 |
Company DUNS | 080813890 |
Company Name | PERIGEN 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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
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 |
Phone | 855-236-4353 |
support@perigen.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00862095000491 [Primary] |
HGM | System, Monitoring, Perinatal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-07 |
Device Publish Date | 2019-10-30 |
00862095000460 | PeriWatch Vigilance Tracings is intended to be used as a complete Obstetrical Data Management Sy |
00862095000446 | PeriWatch Vigilance Tracings is intended to be used as a complete Obstetrical Data Management Sy |
00862095000491 | PeriWatch Vigilance Tracings is intended to be used as a complete Obstetrical Data Management Sy |