| Primary Device ID | 00840828139823 |
| NIH Device Record Key | 590271fd-30d6-4ba9-8434-6df7a7603328 |
| Commercial Distribution Discontinuation | 2017-12-28 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | CBL 060,PH,TW,5LD,YOKE,10FT,AHA,INTERM |
| Version Model Number | CBT-05NB-10CS-3001 |
| Catalog Number | 18673 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| 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 | 1-800-235-7500 |
| mwinter@curbell.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840828139823 [Primary] |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 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 |
| 00840828195546 - GEN4 INTERACTIVE | 2025-12-17 |
| 00840828195553 - GEN4 INTERACTIVE | 2025-12-17 |