| Primary Device ID | 04049188156112 |
| NIH Device Record Key | ae37a848-7d70-4109-813d-d9c84c5b5abf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Leica ST5020 Config. 3 |
| Version Model Number | 14905020US3 |
| Catalog Number | 14905020US3 |
| Company DUNS | 315539452 |
| Company Name | Leica Biosystems Nussloch GmbH |
| 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 | 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 |
| Phone | +4962241430 |
| CHS.support@LeicaBiosystems.co |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 * |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04049188156112 [Primary] |
| KPA | Slide stainer, automated |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-12-17 |
| Device Publish Date | 2018-11-16 |
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