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Sign in to claim this brandPremier Biotech, LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 725 Kasota Ave SE, Minneapolis, MN, 55414
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3010800486
- DUNS Number
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Catalogue (74)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Premier Bio-Cup & Bio-Dip | PBCard-01-BZO300 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-12-02 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-05-04 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-01-AMP500 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-05-09 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-05-04 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-04-13 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-01-PCP | FDA UDI | U | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-10-04 | FDA UDI | Class II | Active |
| OralTox | OT80402 | FDA UDI | Class II | Unknown |
| OralTox | OT80701 | FDA UDI | Class II | Unknown |
| Premier Bio-Cup & Bio-Dip | PBCup-06-04 | FDA UDI | Class II | Active |
| OralTox | OT80602 | FDA UDI | Class II | Unknown |
| Premier Bio-Cup & Bio-Dip | PBCup-13-01 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-06-01 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-10-06 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-03-06 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-10-33 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCup-09-06 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-05-09 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-01-COC150 | FDA UDI | Class II | Active |
| Premier Bio-Cup & Bio-Dip | PBCard-06-23 | FDA UDI | Class II | Active |
| OralTox Oral fluid Drug Test | K181305 | FDA 510(k) | Class II | Active |
| OralTox Oral Fluid Drug Test | K171403 | FDA 510(k) | Class II | Active |
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