| Primary Device ID | 06936189900067 |
| NIH Device Record Key | e4a4c725-33e5-41bf-93c4-6c3f3a936625 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SHARPER IMAGE |
| Version Model Number | 25 in |
| Company DUNS | 548239775 |
| Company Name | GUANGDONG OKAY TECHNOLOGY CO.,LTD. |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06936189900067 [Primary] |
| ISA | Massager, Therapeutic, Electric |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-10-05 |
| Device Publish Date | 2021-09-27 |
| 06936189900067 | 25 in |
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