| Primary Device ID | 00840067102671 |
| NIH Device Record Key | ed6047f7-ad23-4866-9c94-c57547b2f6d3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IOMAX Extender Pod |
| Version Model Number | 362071-000 |
| 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 | 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 | false |
| OTC Over-The-Counter | false |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com | |
| Phone | +1(509)735-6481 |
| applications@cadwell.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840067102671 [Primary] |
| GWF | STIMULATOR, ELECTRICAL, EVOKED RESPONSE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-05-21 |
| Device Publish Date | 2019-05-13 |
| 00840067102671 | 16 Channel Input Extender |
| 00840067102657 | TCS-9 Output Extender |