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Ez Cart Arm Assembly

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5313-00Model 5290-00

by The Magstim Company Limited

Identity

Trade Name
Ez Cart Arm Assembly EUDAMED
HORIZON® Ez Cart Arm Assembly FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Stimulator Cart EUDAMED
Model / Reference
5290-00 EUDAMED
5313-00 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05060229532510 EUDAMEDFDA UDI
Basic UDI-DI
5060229530015W EUDAMED
510(k) Number
K180907 FDA UDI
K182853 FDA UDI
K183376 FDA UDI
FDA Product Code
OBP FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.5805 FDA UDI
Market of Registration
Netherlands 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Device sterilization/disinfection container, reusable

Ez Cart Arm Assembly by The Magstim Company Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000003956
Authorised Representative
Technomed Europe NL-AR-000002048

Sources (2)

  • EUDAMED a895c23c-3f2c-412a-881c-a2901d71c0a9 61 fields · synced Jun 17, 2026
  • FDA UDI 044e3ce8-c454-42fa-ab35-6fdabb47f519 34 fields · synced May 30, 2026