| Primary Device ID | 06430035220021 |
| NIH Device Record Key | e9193d48-5a60-4bf1-a77d-3156c55fb654 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FemiScan |
| Version Model Number | Cover |
| Company DUNS | 369960000 |
| Company Name | Mega Elektroniikka Oy |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +358175817700 |
| mega@megaemg.com | |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06430035220021 [Primary] |
| HIR | Perineometer |
| 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 | 2016-09-22 |
| 06430035220021 | Electrode for FemiScan HomeTrainer (HTCS) device. For single patient use. |
| 06430035220014 | FemiScan device is for monitoring and recording muscle activity of the pelvic floor muscles by u |