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Dialysate Cartridge

FDA UDI

Class II (US FDA UDI)

by Quanta Dialysis Technologies, Ltd.

Identity

Trade Name
Dialysate Cartridge FDA UDI
Generic Name
Haemodialysis system dialysate delivery set FDA UDI
Device Name
Quanta Dialysis System Dialysate Cartridge FDA UDI
Model / Reference
SC-14354 FDA UDI
Description
Quanta Dialysis System Dialysate Cartridge FDA UDI

Identifiers

Primary DI / UDI-DI
05060497260047 FDA UDI
FDA Product Code
KDI FDA UDI
GMDN Term
Haemodialysis system dialysate delivery set 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Haemodialysis system dialysate delivery set

Dialysate Cartridge by Quanta Dialysis Technologies, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis system dialysate delivery set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ebb882b7-930e-49a1-8c20-b20ffdd71b2a 33 fields · synced May 30, 2026