DEVICE: Charger (00847946019976)
Device Identifier (DI) Information
Charger
1119-0500-66
In Commercial Distribution
Zoll Medical Corporation
1119-0500-66
In Commercial Distribution
Zoll Medical Corporation
SUREPOWER CHARGING STATION, REFURB
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| No | |
| No | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 17115 | Noninvasive device battery charger |
An electrically-powered device designed to supply an electrical charge, via a direct/wired or wireless connection, to the battery of a noninvasive device to recharge it for operation; it is not intended to receive data from and transmit data to other devices (i.e., not a transceiver). It is typically in the form of an electronic circuitry housing with a cable.
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| NSX | Software, transmission and storage, patient data |
| LDD | Dc-defibrillator, low-energy, (including paddles) |
| DXN | SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE |
| MKJ | Automated external defibrillators (non-wearable) |
| DSK | COMPUTER, BLOOD-PRESSURE |
| LIX | Aid, cardiopulmonary resuscitation |
| DRO | PACEMAKER, CARDIAC, EXTERNAL TRANSCUTANEOUS (NON-INVASIVE) |
| DQA | Oximeter |
| DRT | MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM) |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K142915 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Atmospheric Pressure: more than 0 KiloPascal |
| Storage Environment Temperature: exactly 0 Degrees Celsius |
| Handling Environment Temperature: exactly 0 Degrees Celsius |
| Storage Environment Humidity: exactly 0 Percent (%) Relative Humidity |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| No Device Sizes |
Device Record Status
f2d0a2b1-1295-4c4d-81da-964356c48ada
February 06, 2020
4
September 06, 2017
February 06, 2020
4
September 06, 2017
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined