| Primary Device ID | 10840828180556 |
| NIH Device Record Key | f6854e55-7af8-4ba7-b339-6bfd206ac1be |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DISP NLCR COMPAT SPO2 SNSR,NON OXMX,D-25 |
| Version Model Number | CSA001DA-P100 |
| Catalog Number | 26230 |
| Company DUNS | 796452311 |
| Company Name | CURBELL MEDICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840828180559 [Primary] |
| GS1 | 00840828189361 [Package] Contains: 00840828180559 Package: Case [24 Units] In Commercial Distribution |
| GS1 | 10840828180556 [Package] Contains: 00840828180559 Package: [30 Units] In Commercial Distribution |
| DQA | Oximeter |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-12 |
| Device Publish Date | 2020-08-04 |
| 00840828195805 - GEN4 INTERACTIVE | 2025-12-24 |
| 00840828195812 - RESPONDER 5, INTERACTIVE | 2025-12-24 |
| 00840828195485 - RESPONDER 5, INTERACTIVE | 2025-12-17 |
| 00840828195492 - RESPONDER 5, INTERACTIVE | 2025-12-17 |
| 00840828195508 - GEN4 INTERACTIVE | 2025-12-17 |
| 00840828195515 - GEN4 INTERACTIVE | 2025-12-17 |
| 00840828195522 - GEN4 INTERACTIVE | 2025-12-17 |
| 00840828195539 - GEN4 INTERACTIVE | 2025-12-17 |