| Primary Device ID | 20883873824638 |
| NIH Device Record Key | dd55f18b-009a-4299-ad2a-b30ae21fc60d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 50MM WIDE ECG PAPERRECORDING, UDI |
| Version Model Number | 11240 |
| Catalog Number | 11240-000031 |
| Company DUNS | 009251992 |
| Company Name | PHYSIO-CONTROL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00883873824634 [Primary] |
| GS1 | 20883873824638 [Primary] |
| GS1 | 50883873824639 [Package] Package: case [50 Units] In Commercial Distribution |
| DSF | RECORDER, PAPER CHART |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-11 |
| Device Publish Date | 2024-06-03 |