Identity
- Trade Name
- Homechoice Claria FDA UDI
- Generic Name
- Peritoneal dialysis system FDA UDI
- Device Name
- Homechoice Claria Automated Peritoneal Dialysis Cycler FDA UDI
- Model / Reference
- 5C6M40 FDA UDI
- Description
- Homechoice Claria Automated Peritoneal Dialysis Cycler FDA UDI
Identifiers
- Catalog Number
- 5C6M40 FDA UDI
- Primary DI / UDI-DI
- 00085412676463 FDA UDI
- 510(k) Number
- K201867 FDA UDI
- FDA Product Code
- FKX FDA UDI
- GMDN Term
- Peritoneal dialysis system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5630 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
Yes
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: Peritoneal dialysis system
Homechoice Claria by Baxter Healthcare Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Baxter Healthcare Corp
Sources (1)
- FDA UDI 01893c09-cf88-4abc-82dd-e44e065ebea9 37 fields · synced May 30, 2026