| Primary Device ID | 08592566679001 |
| NIH Device Record Key | e640c55a-b62a-46e3-825a-a3b014d47bb5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FlexiCAP electrode ring - rubber |
| Version Model Number | white |
| Catalog Number | 67-900 |
| Company DUNS | 495566056 |
| Company Name | DEYMED Diagnostic s.r.o. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08592566679001 [Primary] |
| HCC | Device, Biofeedback |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-03 |
| Device Publish Date | 2023-10-26 |
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