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Coriton

FDA UDI

Class I (US FDA UDI)

by CORITON Instrument Co., Ltd

Identity

Trade Name
CORITON FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Roll Stand for Infusion Pump FDA UDI
Model / Reference
E.W.TB.RS003 FDA UDI
Description
Roll Stand for Infusion Pump FDA UDI

Identifiers

Catalog Number
RS003 FDA UDI
Primary DI / UDI-DI
06973456940289 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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: Electromechanical device/system transport trolley

Coriton by CORITON Instrument Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CORITON Instrument Co., Ltd

Sources (1)

  • FDA UDI b8f04631-93da-4d3e-8c7b-a5f4b2c2a82c 35 fields · synced May 30, 2026