← Back to catalogue

Wall mount

EUDAMEDFDA UDI

Class I (EU MDR)

Ref WM500Model WM001,WM001E,WM300,WM500,WM600,WM700,WM800Ref WM500-100

by CORITON Instrument Co., Ltd.

Identity

Trade Name
Wall mount EUDAMED
CORITON FDA UDI
Generic Name
Custom-made medical device mount FDA UDI
Device Name
Wall mount EUDAMED
Patient Monitor Wall Mount FDA UDI
Model / Reference
WM001,WM001E,WM300,WM500,WM600,WM700,WM800 EUDAMED
WM500 EUDAMED
WM500-100 EUDAMEDFDA UDI
Description
Patient Monitor Wall Mount FDA UDI

Identifiers

Catalog Number
WM500 FDA UDI
Primary DI / UDI-DI
06973456940067 EUDAMED
06973456940128 EUDAMEDFDA UDI
Basic UDI-DI
697345694WM68 EUDAMED
Direct Marketing DI
06973456940067 EUDAMED
06973456940128 EUDAMED
FDA Product Code
FOX FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Custom-made medical device mount FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6990 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Device sterilization/disinfection container, reusable

Wall mount by Coriton Instrument Co., Ltd. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001572
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (3)

  • EUDAMED dbc30098-1f09-4fdd-933e-aaac178c075c 61 fields · synced Jul 9, 2026
  • EUDAMED f1307bf1-8185-4872-8a47-5a0297d989dd 61 fields · synced May 18, 2026
  • FDA UDI 344bda31-fb6f-41ad-9804-851188d63c87 35 fields · synced May 26, 2026