FDA UDI
In Commercial Distribution
🇺🇸 United States
PEDI-PADZ
DI: 00847946016425
·
Model: 8900-2500-01
·
Zoll Medical Corporation
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- PEDI-PADZ
- Primary DI
- 00847946016425
- Version / Model
- 8900-2500-01
- Company Name
- Zoll Medical Corporation
- Labeler DUNS
- 055363428
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2014-09-24
- Public Version
- 3
- Public Version Date
- 2022-02-08
- Public Version Status
- Update
- Public Device Record Key
- 734ee28c-1365-4033-9769-4bd83b317f57
Device Description
ELECTRODES, PEDI-PADZ, SOLID GEL W/10 FT LEADWIRES, SINGLE
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DRK | Dc-defibrillator, high energy, (including paddles) | Cardiovascular | 870.5300 | 3 |
| MKJ | Automated external defibrillators (non-wearable) | Cardiovascular | 870.5310 | 3 |
| LDD | Dc-defibrillator, low-energy, (including paddles) | Cardiovascular | 870.5300 | 2 |
| DRO | PACEMAKER, CARDIAC, EXTERNAL TRANSCUTANEOUS (NON-INVASIVE) | Cardiovascular | 870.5550 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 48048 | Rechargeable professional automated external defibrillator | A portable electronic device designed to automatically detect cardiac arrhythmias (ventricular fibrillation/pulseless ventricular tachycardia) in a sudden cardiac arrest (SCA) patient, after which it audibly/visually instructs an operator to enable it to activate defibrillation of the heart through application of electrical shocks to the chest surface. The device is intended to be operated by healthcare professionals (e.g., paramedics, medical staff) in healthcare settings. It consists of an external pulse generator (EPG) and a pair of skin-adhesive electrodes to monitor the rhythm and deliver the shocks; it also includes internal rechargeable batteries that must be charged when not in use. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00847946016425 | GS1 | ||||
| Package | 10847946016422 | GS1 | CASE | 6 | In Commercial Distribution |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 10.3" X 8.5" X 1.0" |
Storage Conditions
- Type
- Handling Environment Temperature
- Temperature Range
- 0 – 50 Degrees Celsius
- Type
- Storage Environment Temperature
- Temperature Range
- 0 – 35 Degrees Celsius