FDA Registration
Active
🇯🇵 Japan
Hemato Check Module
Reg #: 8010061
·
FEI: 3002807736
·
Expires 2025
Products
1
Proprietary Names
1
Establishment Types
2
Classifications
1
Registration Details
- Registration Name
- NIHON SEIMITSU SOKKI CO., LTD.
- Registration Number
- 8010061
- FEI Number
- 3002807736
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 2508-13 NAKAGO
- City
- SHIBUKAWA Gunma
- Country
- JP
Owner / Operator
- Firm Name
- NIHON SEIMITSU SOKKI CO., LTD.
- Operator Number
- 8010061
- Address
- 2508-13 NAKAGO
- City
- SHIBUKAWA, GUNMA
- State
- JP-NOTA
- Postal Code
- 377-0293
- Country
- JP
- Correspondent
- HIDEKI SATO
US Agent
- Business Name
- FLORENCE ROSTAMI LAW, LLC
- Contact Name
- FLORENCE ROSTAMI
- Address
- 420 Lexington Ave Rm 1402
- City
- New York
- State
- NY
- ZIP
- 10170
- Country
- US
- [email protected]
- Phone
- 212 2093962
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Diazonium Colorimetry, Urobilinogen (Urinary, Non-Quant.) | CDM | Class 1 | Clinical Chemistry | No | 2023-07-30 |
Proprietary Names
Hemato Check Module
Establishment Types
Develop Specifications But Do Not Manufacture At This Facility
Manufacture Medical Device