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Hydroven

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 316AI78Model 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
78CM ARM INSERT FDA UDI
Model / Reference
526000-03 EUDAMED
316AI78 EUDAMEDFDA UDI
Description
78CM ARM INSERT FDA UDI

Identifiers

Catalog Number
316AI78 FDA UDI
Primary DI / UDI-DI
05051968031457 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 9380e971-c99f-4207-aa6e-43d517432885 61 fields · synced Jun 18, 2026
  • FDA UDI cd779471-143f-4d5d-9ff5-a5ea7e13375d 36 fields · synced May 30, 2026