Identity
- Trade Name
- CIM med GmbH FDA UDI
- Generic Name
- Medical monitor/light mount FDA UDI
- Device Name
- Support arm Pivot grounded 300, 5" plunge plate, adapter anaesthesia machines with side channel FDA UDI
- Model / Reference
- A-230A-4K.gr1 FDA UDI
- Description
- Support arm Pivot grounded 300, 5" plunge plate, adapter anaesthesia machines with side channel FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04061162030881 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- CIM med GmbH
Sources (1)
- FDA UDI f86577d3-f06f-403c-a5ce-be2968af0fca 34 fields · synced Jun 8, 2026