Primary Device ID | B087HUB01021 |
NIH Device Record Key | 4b462041-426e-4fc7-ac46-88d84fbbd07a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PeriWatch™ HUB™ |
Version Model Number | 01.02.xx |
Company DUNS | 533337713 |
Company Name | PERIGEN SOLUTIONS LTD |
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 | true |
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 | 8663216788 |
support@perigen.com | |
Phone | 8663216788 |
support@perigen.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B087HUB01021 [Primary] |
HGM | System, Monitoring, Perinatal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-25 |
Device Publish Date | 2018-09-16 |
B087HUB01021 | PeriCALM® Tracings™ is intended for use as a central monitoring system with signal analysis a |
B087HUB01011 | PeriCALM® Tracings™ is intended for use as a central monitoring system with signal analysis a |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERIWATCH 87307470 5408773 Live/Registered |
PeriGen, Inc. 2017-01-19 |