FDA Registration
Active
🇯🇵 Japan
Nipro SafeTouch TULIP Safety AVF
Reg #: 3000247873
·
FEI: 3000247873
·
Expires 2025
Products
3
Proprietary Names
1
Establishment Types
1
Classifications
3
Registration Details
- Registration Name
- NIPRO CORPORATION
- Registration Number
- 3000247873
- FEI Number
- 3000247873
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 3-26, Senriokashinmachi, Settsu, --
- City
- Osaka
- Country
- JP
Regulatory Submissions
- 510(k) Number
- K071145
Owner / Operator
- Firm Name
- NIPRO CORPORATION
- Operator Number
- 8030375
- Address
- 3-26, Senriokashinmachi, Settsu,, --
- City
- Osaka
- State
- JP-27
- Postal Code
- 566-8510
- Country
- JP
- Correspondent
- Nobuhiro Morimoto
US Agent
- Business Name
- NIPRO MEDICAL CORPORATION
- Contact Name
- JESSICA OSWALD-MCLEOD
- Address
- 3150 NW 107th Ave
- City
- Doral
- State
- FL
- ZIP
- 33172
- Country
- US
- [email protected]
- Phone
- 305 4326699
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Catheter, Hemodialysis, Non-Implanted | MPB | Class 2 | Gastroenterology, Urology | No | 2007-11-15 |
| Accessories, Blood Circuit, Hemodialysis | KOC | Class 2 | Gastroenterology, Urology | No | 2007-11-15 |
| System, Blood, Extracorporeal And Accessories | LLB | Class 2 | Gastroenterology, Urology | No | 2007-11-15 |
Proprietary Names
Nipro SafeTouch TULIP Safety AVF
Establishment Types
Export Device to the United States But Perform No Other Operation on Device