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Citrasate

FDA UDI

Class II (US FDA UDI)

by Fresenius Medical Care Renal Therapies Group, LLC

Identity

Trade Name
Citrasate FDA UDI
Generic Name
Haemodialysis concentrate FDA UDI
Device Name
Citrasate Liquid Acid Concentrate for Bicarbonate Dialysis, Case FDA UDI
Model / Reference
08-2251-CA FDA UDI
Description
Citrasate Liquid Acid Concentrate for Bicarbonate Dialysis, Case FDA UDI

Identifiers

Catalog Number
08-2251-CA FDA UDI
Primary DI / UDI-DI
00840861101344 FDA UDI
FDA Product Code
KPO FDA UDI
GMDN Term
Haemodialysis concentrate FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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

No

FDA UDI

Category: Haemodialysis concentrate

Citrasate by Fresenius Medical Care Renal Therapies Group, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis concentrate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61ec9b36-6d17-423d-a93d-495d80b34fd5 36 fields · synced Jun 8, 2026