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Roll Stand for Medical Equipment

EUDAMEDFDA UDI

Class I (EU MDR)

Ref RS001-01-WNModel RS001,RS001E,RS001C,RS002,RS002C,RS003,RS010,RS011C,RS010C,RS011,RS008,RS008S,SUN008,SUN009,SUN010

by CORITON Instrument Co., Ltd.

Identity

Trade Name
Roll Stand for Medical Equipment EUDAMED
CORITON FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Roll Stand EUDAMED
Roll Stand for Medical Device FDA UDI
Model / Reference
RS001,RS001E,RS001C,RS002,RS002C,RS003,RS010,RS011C,RS010C,RS011,RS008,RS008S,SUN008,SUN009,SUN010 EUDAMED
RS001-01-WN EUDAMEDFDA UDI
Description
Roll Stand for Medical Device FDA UDI

Identifiers

Catalog Number
RS001 FDA UDI
Primary DI / UDI-DI
06973456941415 EUDAMEDFDA UDI
Basic UDI-DI
697345694RS65 EUDAMED
Direct Marketing DI
06973456941415 EUDAMED
FDA Product Code
FOX 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 EUDAMEDFDA UDI
Regulation Number
880.6990 FDA UDI
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

Roll Stand for Medical Equipment 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

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Manufacturer

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

Sources (2)

  • EUDAMED 58ea3d73-a207-4b36-aceb-aee9c69e81a0 61 fields · synced Jun 18, 2026
  • FDA UDI e78a3f5e-ce5f-4972-9c21-5df942ddc988 35 fields · synced May 29, 2026