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Ventilator arm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref AR105Model AR102,AR105,SUN-AR103

by CORITON Instrument Co., Ltd.

Identity

Trade Name
Ventilator arm EUDAMED
CORITON FDA UDI
Generic Name
Custom-made medical device mount FDA UDI
Device Name
Ventilator arm EUDAMED
Ventilator Support Arm FDA UDI
Model / Reference
AR102,AR105,SUN-AR103 EUDAMED
AR105 EUDAMEDFDA UDI
Description
Ventilator Support Arm FDA UDI

Identifiers

Catalog Number
AR105 FDA UDI
Primary DI / UDI-DI
06973456941811 EUDAMEDFDA UDI
Basic UDI-DI
697345694AR4G EUDAMED
Direct Marketing DI
06973456941811 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

Ventilator arm 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 (2)

  • EUDAMED 21b82c0d-525b-4341-9043-4e712f7857b3 61 fields · synced Jun 19, 2026
  • FDA UDI f0564911-db43-4458-8c27-9b2f2d2f82f2 35 fields · synced May 30, 2026