| Primary Device ID | 10847946016354 |
| NIH Device Record Key | 8fb9ef8e-8e33-4af4-80fd-f4c1f31b0662 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PEDI PADZ II |
| Version Model Number | 8900-1005-01 |
| Company DUNS | 055363428 |
| Company Name | Zoll Medical Corporation |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10847946016354 [Primary] |
| MKJ | Automated External Defibrillators (Non-Wearable) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-19 |
| Device Publish Date | 2026-02-11 |
| 10847946021327 - Cuffs | 2026-02-23 neonate cuffs package level |
| 10847946021334 - Cuffs | 2026-02-23 neonate cuffs package level |
| 10847946021341 - Cuffs | 2026-02-23 neonate cuffs package level |
| 10847946021358 - Cuffs | 2026-02-23 neonate cuffs package level |
| 10847946021365 - Cuffs | 2026-02-23 neonate cuffs package level |
| 10847946016354 - PEDI PADZ II | 2026-02-19PEDI-PADZ RADIOLUCENT SOLID GEL ELECTRODE (P/N 8900-1007-01), 6/CASE |
| 10847946016354 - PEDI PADZ II | 2026-02-19 PEDI-PADZ RADIOLUCENT SOLID GEL ELECTRODE (P/N 8900-1007-01), 6/CASE |
| 10847946016422 - PEDI PADZ | 2026-02-19 PEDI-PADZ SOLID GEL ELECTRODES, W/10 FT LEADWIRES, 6 PER CASE |
| 00847946053932 - AED PLUS | 2026-02-11 AED PLUS, PS SERIES W/AED CVR, LCD, NO VOICE RCDG, NO GRAPHICS, ENG |