| Primary Device ID | EJKP100003786A0 |
| NIH Device Record Key | c1df1c19-6846-4cf2-956a-0a7c7e1e705d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ergoline Vitality Hybrid Light 3 |
| Version Model Number | JK 164 / 50-4 HLT-3 TT |
| Company DUNS | 316232073 |
| Company Name | JK-Products GmbH |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EJKP100003786A0 [Primary] |
| LEJ | Booth, Sun Tan |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-09 |
| Device Publish Date | 2022-08-01 |
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