Primary Device ID | 10815098020482 |
NIH Device Record Key | f28fc7ac-316c-43d4-b348-f3c569e4ad47 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DDU-1XX Series Adult Pads Adapter, Zoll Configuration |
Version Model Number | DAC-310E |
Company DUNS | 128340200 |
Company Name | DEFIBTECH, L.L.C. |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10815098020482 [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 | 4 |
Public Version Date | 2024-06-06 |
Device Publish Date | 2015-10-24 |
10815098020475 - DDU-1XX Series Adult Pads Adapter, Physio-Control Configuration | 2024-06-06 |
10815098020482 - DDU-1XX Series Adult Pads Adapter, Zoll Configuration | 2024-06-06 |
10815098020482 - DDU-1XX Series Adult Pads Adapter, Zoll Configuration | 2024-06-06 |
10815098020499 - DDU-1XXX/2XXX Adult Pads Adapter, Physio-Control Configuration | 2024-06-06 |
10815098020505 - DDU-1XXX/2XXX Adult Pads Adapter, Zoll Configuration | 2024-06-06 |
10815098020512 - DDU-2XXX Series ECGMA Cable, AAMI Configuration | 2024-06-06 |
10815098020529 - DDU-2XXX Series ECGMA Cable, IEC Configuration | 2024-06-06 |
10815098020437 - DDU-1XX Series Pediatric Pads Configuration | 2023-07-06 |
10815098020451 - DDU-1XXX/2XXX Series Pediatric Pads Configuration | 2023-07-06 |