| Primary Device ID | 20840067101401 |
| NIH Device Record Key | 9d93a824-0d82-44f3-bb2c-3128b9d0bf1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cadwell Disposable Disc Electrodes |
| Version Model Number | 302290-000 |
| Company DUNS | 098554157 |
| Company Name | CADWELL INDUSTRIES, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(509)735-6481 |
| applications@cadwell.com |
| Outer Diameter | 0.75 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840067101407 [Primary] |
| GS1 | 10840067101404 [Package] Contains: 00840067101407 Package: Box [20 Units] In Commercial Distribution |
| GS1 | 20840067101401 [Package] Contains: 10840067101404 Package: Case [12 Units] In Commercial Distribution |
| GXY | ELECTRODE, CUTANEOUS |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-10-22 |
| Device Publish Date | 2016-09-05 |
| 20840067101418 | 302291-000 |
| 20840067101401 | 302290-000 |
| 10840067101411 | 302291-000 |