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Hmb32

FDA UDI

Class II (US FDA UDI)

by Haemopharm Biofluids Srl

Identity

Trade Name
HMB32 FDA UDI
Generic Name
Haemodialysis dialysate solution FDA UDI
Device Name
dialysis solution,ml 500+1500 each FDA UDI
Model / Reference
MD042 FDA UDI
Description
dialysis solution,ml 500+1500 each FDA UDI

Identifiers

Primary DI / UDI-DI
38051411600061 FDA UDI
FDA Product Code
KPO FDA UDI
GMDN Term
Haemodialysis dialysate solution 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

Yes

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

Dimensions & Sizes

Size
Total Volume — 2000 Milliliter FDA UDI

Category: Haemodialysis dialysate solution

Hmb32 by Haemopharm Biofluids Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis dialysate solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9779b9c6-6e49-483b-b7b5-d6d2eebe2403 36 fields · synced Jun 8, 2026