Primary Device ID | 00850490007504 |
NIH Device Record Key | 288ff6dd-3dfa-4c81-bc0f-ac76560b17ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VistaPhone Compact Cardiac Monitoring Kit |
Version Model Number | 1500-01 |
Catalog Number | 1400-02 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850490007504 [Primary] |
DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency |
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 | 2023-03-31 |
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