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Hydroven

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 5103L66Model 526000-03

by ArjoHuntleigh AB

Identity

Trade Name
HYDROVEN EUDAMEDFDA UDI
Generic Name
Multi-chamber venous compression system garment, reusable FDA UDI
Device Name
ACS900 PUMP UK STD TUBE SET EUDAMED
LEG ASSY CONSOLE 66CM HYDROVEN FDA UDI
Model / Reference
526000-03 EUDAMED
5103L66 EUDAMEDFDA UDI
Description
LEG ASSY CONSOLE 66CM HYDROVEN FDA UDI

Identifiers

Catalog Number
5103L66 FDA UDI
Primary DI / UDI-DI
05051968031273 EUDAMEDFDA UDI
Basic UDI-DI
5060693520013VG EUDAMED
FDA Product Code
JOW FDA UDI
EMDN Code
Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED
GMDN Term
Multi-chamber venous compression system garment, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Hydroven by Arjohuntleigh AB — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (2)

  • EUDAMED 51e112f6-48b4-4f1f-aa61-3e467216cd53 61 fields · synced Jul 20, 2026
  • FDA UDI 6c087515-24eb-422c-87de-f9a568e316fd 36 fields · synced May 30, 2026