Primary Device ID | 00847946028275 |
NIH Device Record Key | 398f651a-7d0d-433b-bf63-16a5c47ba190 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ResQStrap |
Version Model Number | 12-0392-000 |
Company DUNS | 055363428 |
Company Name | Zoll Medical Corporation |
Device Count | 1 |
DM Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00847946028275 [Primary] |
BTK | STRAP, HEAD, GAS MASK |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-02 |
Device Publish Date | 2020-06-24 |
00847946096168 - AED PLUS | 2024-04-05 AED PLUS, PS SERIES, W/AED CVR, LCD, NO VOICE RECORDING, ENGLISH, REFURB |
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00847946096212 - AED PLUS | 2024-04-05 AED PLUS, PS SERIES W/BASIC CVR, LCD, VOICE RCDG, ENG, REFURB |
00847946096229 - AED PLUS | 2024-04-05 AED PLUS, PS SERIES W/AED CVR, LCD, VOICE RCDG, ENG, REFURB |
00847946096243 - AED PLUS | 2024-04-05 AED PLUS, PS SERIES NO GRAPHICS, W/AED CVR, LCD, VOICE RCDG, ENG |
00847946096298 - AED PRO | 2024-04-05 AED PRO, SEMI AUTOMATIC ONLY, NO BATTERY, NO ELECTRODES, REFURB |
00847946096472 - AED PRO | 2024-04-05 AED PRO, SEMI AUTO W/MNL OVERRIDE, NO VOICE, LCD, ENGLISH, REFURB |
00847946096533 - AED PLUS | 2024-04-05 AED PLUS, PA SERIES, NO LCD, NO VOICE RCDG, ENG, REFURB |