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HistoSonics

FDA UDI

Class I (US FDA UDI)

by Histosonics, Inc

Identity

Trade Name
HistoSonics FDA UDI
Generic Name
Combination water purification system FDA UDI
Device Name
Fluidics Disposable Kit FDA UDI
Model / Reference
HISFK2001 FDA UDI
Description
Fluidics Disposable Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00850006962075 FDA UDI
FDA Product Code
JRS FDA UDI
GMDN Term
Combination water purification system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Combination water purification system

HistoSonics by Histosonics, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Combination water purification system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Histosonics, Inc

Sources (1)

  • FDA UDI d631a383-4baf-41cf-9c7e-6676c1106818 35 fields · synced May 30, 2026