← Back to catalogue

CIM med GmbH

FDA UDI

Class I (US FDA UDI)

by CIM med GmbH

Identity

Trade Name
CIM med GmbH FDA UDI
Generic Name
Medical monitor/light mount FDA UDI
Device Name
Support arm Pivot grounded 240, tray 300x300mm, adapter vertical wall channel FDA UDI
Model / Reference
A-224E-4V.2_3030T FDA UDI
Description
Support arm Pivot grounded 240, tray 300x300mm, adapter vertical wall channel FDA UDI

Identifiers

Primary DI / UDI-DI
04061162090489 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Medical monitor/light mount FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

CIM med GmbH by CIM med GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
CIM med GmbH

Sources (1)

  • FDA UDI c312a437-f54f-4573-b8a2-fd8d7ad0baa5 34 fields · synced May 31, 2026