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Acid Dissolution System

FDA UDI

Class II (US FDA UDI)

by Isopure, Corp.

Identity

Trade Name
Acid Dissolution System FDA UDI
Generic Name
Haemodialysis concentrate FDA UDI
Device Name
Dialysate Concentrate For Hemodialysis (Liquid or Powder) FDA UDI
Model / Reference
MD70510 FDA UDI
Description
Dialysate Concentrate For Hemodialysis (Liquid or Powder) FDA UDI

Identifiers

Primary DI / UDI-DI
00852456007115 FDA UDI
510(k) Number
K191093 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

No

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 concentrate

Acid Dissolution System by Isopure, Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis concentrate.

Cleared under the same submission

K191093 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Isopure, Corp.

Sources (1)

  • FDA UDI d8b5a377-48ea-43b9-ac05-f38ff756f82b 34 fields · synced May 30, 2026