| Primary Device ID | 00883873762370 |
| NIH Device Record Key | 20c53701-d8ca-4d74-ba8c-6242c28ec1f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LUCAS CHEST COMPRESSION SYSTEM |
| Version Model Number | 99576 |
| Catalog Number | 99576-000043U |
| 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 | true |
| Manufacturing Date | true |
| 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 | |
| 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 | 00883873762370 [Primary] |
| DRM | Compressor, cardiac, external |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-10 |
| Device Publish Date | 2024-05-31 |