| Primary Device ID | 00840828125413 |
| NIH Device Record Key | af9f29e3-6913-4a43-acc1-8dffdf224a16 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CBL 024,PLP,MULTILINK,5LEAD,YOKE,10FT,A |
| Version Model Number | CBT-05JD-10CM-0121 |
| Catalog Number | 5661 |
| 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 | 00840828125413 [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 |
| 00840828187381 - SURE LOCK, ASSEMBLY, A34, RED LEVER | 2025-04-02 SURE LOCK, ASSEMBLY, A34, RED LEVER |
| 00840828187404 - SURE LOCK, ASSEMBLY, A34, ORANGE LEVER | 2025-04-02 SURE LOCK, ASSEMBLY, A34, ORANGE LEVER |
| 00840828194204 - GEN4 AUSTCO TACERA ENTERTAINMENT | 2025-03-14 |
| 00840828194211 - GEN4 PLUS, DIRECT ACCESS | 2025-03-14 |
| 00840828194280 - GEN4 INTERACTIVE | 2025-03-14 |
| 00840828194297 - GEN4 INTERACTIVE | 2025-03-14 |
| 00840828194303 - GEN4 INTERACTIVE | 2025-03-14 |
| 00840828194228 - REGO 1.1,PID,NO AUX,14' | 2025-03-07 |