Primary Device ID | 00847946016692 |
NIH Device Record Key | 80c292b3-cd1a-4ae3-a595-45cf44f6fd3d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ZOLL MFC |
Version Model Number | 1001-0196-02 |
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 | 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 |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 0 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00847946016692 [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 | 2014-09-24 |
00847946099671 | CABLE ASSY, MFC-CPRD, X SERIES |
00847946018320 | 1009-0913-05 |
00847946018313 | 1009-0913-04 |
00847946016807 | 1007-0196-01 |
00847946016777 | 1009-0913-03 |
00847946016692 | 1001-0196-02 |
00847946055998 | CABLE ASSY, MFC-CPRD, X SERIES |