Primary Device ID | 00852132007408 |
NIH Device Record Key | efc0d659-74da-4eff-bf1c-ee7ef711b982 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BodyGuardian Kit |
Version Model Number | L-44 |
Company DUNS | 859807815 |
Company Name | PREVENTICE TECHNOLOGIES, 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 | false |
Lot Batch | false |
Serial Number | true |
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 | 00850028319024 [Previous] |
GS1 | 00852132007408 [Primary] |
DSI | Detector And Alarm, Arrhythmia |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-13 |
Device Publish Date | 2024-12-05 |
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