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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
VESA 75/100 fix, adapter vertical wall channel FDA UDI
Model / Reference
S-G-4Z.gr1 FDA UDI
Description
VESA 75/100 fix, adapter vertical wall channel FDA UDI

Identifiers

Primary DI / UDI-DI
04061162007630 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
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

Category: Medical monitor/light mount

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

Similar devices

Also classified as Medical monitor/light mount.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CIM med GmbH

Sources (1)

  • FDA UDI 3fcb6742-019e-4421-8436-3a4eae472369 33 fields · synced Jun 1, 2026