FDA Registration
Active
🇲🇺 Mauritius
MOHE BioTech Production (Mauritius) Ltd.
Reg #: 3043534289
·
FEI: 3043534289
·
Expires 2026
Products
10
Proprietary Names
1
Establishment Types
3
Classifications
10
Registration Details
- Registration Name
- MOHE BioTech Production (Mauritius) Ltd.
- Registration Number
- 3043534289
- FEI Number
- 3043534289
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- The dot Avenue DE TELFAIRE
- City
- MOKA
- Country
- MU
Owner / Operator
- Firm Name
- MOHE BioTech (USA) LLC
- Operator Number
- 10095048
- Address
- 5900 Balcones Drive, STE 100
- City
- Austin
- State
- TX
- Postal Code
- 78731
- Country
- US
- Correspondent
- Claire A Cooper
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Test, Amphetamine, Employment And Insurance Testing, Exempt | PUX | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Opiates, Employment And Insurance Testing, Exempt | PVH | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Barbiturate, Employment And Insurance Testing, Exempt | PUY | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Morphine, Employment And Insurance Testing, Exempt | PVG | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Tricyclic Antidepressant Drugs, Employment And Insurance Testing, Exempt | PVK | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Methadone, Employment And Insurance Testing, Exempt | PVE | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Benzodiazepine, Employment And Insurance Testing, Exempt | PUZ | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Methamphetamine, Employment And Insurance Testing, Exempt | PVD | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Cocaine And Cocaine Metabolite, Employment And Insurance Testing, Exempt | PVA | Class 2 | Clinical Toxicology | No | 2026-02-02 |
| Test, Cannabinoid, Employment And Insurance Testing, Exempt | PVJ | Class 2 | Clinical Toxicology | No | 2026-02-02 |
Proprietary Names
mTest DOA (Urine)
Establishment Types
Complaint File Establishment per 21 CFR 820.198
Manufacture Medical Device
Manufacture Medical Device for Another Party (Contract Manufacturer)