Identity
- Trade Name
- Quanta Dialysis System FDA UDI
- Generic Name
- Haemodialysis system, institutional/home-use FDA UDI
- Device Name
- Quanta Dialysis System Hemodialysis Delivery Device FDA UDI
- Model / Reference
- SC-13940 FDA UDI
- Description
- Quanta Dialysis System Hemodialysis Delivery Device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060497260160 FDA UDI
- 510(k) Number
- K222067 FDA UDI
- FDA Product Code
- KDI FDA UDI
- GMDN Term
- Haemodialysis system, institutional/home-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Haemodialysis system, institutional/home-use
Quanta Dialysis System by Quanta Dialysis Technologies, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- NXSTAGE SYSTEM ONE — NxStage Medical, Inc. · Class II
Cleared under the same submission
K222067 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Quanta Dialysis Technologies, Ltd.
Sources (1)
- FDA UDI 0001bf37-79eb-488d-8a6a-109540bf6601 34 fields · synced May 30, 2026