Primary Device ID | 00847946016678 |
NIH Device Record Key | 1802a3f1-6d08-4b36-a6b2-cb7aa634bea2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ZOLL BATTERY SLA |
Version Model Number | 1001-0144 |
Company DUNS | 055363428 |
Company Name | Zoll Medical Corporation |
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 | 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 | false |
OTC Over-The-Counter | false |
Handling Environment Temperature | Between 0 Degrees Celsius and 0 Degrees Celsius |
Handling Environment Temperature | Between 0 Degrees Celsius and 0 Degrees Celsius |
Handling Environment Temperature | Between 0 Degrees Celsius and 0 Degrees Celsius |
Handling Environment Temperature | Between 0 Degrees Celsius and 0 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00847946016678 [Primary] |
MKJ | Automated external defibrillators (non-wearable) |
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 | 2014-09-23 |
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