Primary Device ID | 00850490007085 |
NIH Device Record Key | 8cbc9e67-931b-4bab-af76-37dbd070d93c |
Commercial Distribution Discontinuation | 2017-04-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | "VitalPatch™ Active Patch |
Version Model Number | 3002-01 |
Company DUNS | 944642730 |
Company Name | Vital Connect, 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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850490007078 [Primary] |
GS1 | 00850490007085 [Package] Contains: 00850490007078 Package: [5 Units] Discontinued: 2017-04-30 Not in Commercial Distribution |
MHX | Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-23 |
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