| Primary Device ID | 00840067102725 |
| NIH Device Record Key | d8c27577-94bd-4312-9a5b-7fa12bd771f9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cadwell Gold Cup Electrode |
| Version Model Number | 203104-200 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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(509)735-6481 |
| applications@cadwell.com |
| Length | 36 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840067102725 [Primary] |
| GXY | ELECTRODE, CUTANEOUS |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-27 |
| Device Publish Date | 2020-02-19 |
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