| Primary Device ID | 00883873782224 |
| NIH Device Record Key | ed695209-2c85-436a-9f60-6da26579f973 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SHIP KIT, POWER SUPPLY,LP35 |
| Version Model Number | 41335 |
| Catalog Number | 41335-000001 |
| Company DUNS | 009251992 |
| Company Name | PHYSIO-CONTROL, INC. |
| 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 | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com | |
| Phone | +1(800)442-1142 |
| rs.seacustomersupport@stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00883873782224 [Primary] |
| MPD | Auxiliary power supply (AC or DC) for low-energy dc-defibrillator |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-28 |
| Device Publish Date | 2024-06-20 |