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LED 150FP Lamp and suspension arm only (for use with a Kenex celling radiation …
EUDAMEDFDA UDIClass I (EU MDR)
Ref 300/L-LED150FP
Identity
- Trade Name
- LED 150FP Lamp and suspension arm only (for use with a Kenex celling radiation shield) inclu PSU EUDAMEDKENEX FDA UDI
- Generic Name
- Fixed examination/treatment room light FDA UDI
- Device Name
- Overhead examination/operating lighting EUDAMEDLED 150FP Lamp and suspension arm only (for use with a Kenex celling radiation shield) inclu PSU FDA UDI
- Model / Reference
- 300/L-LED150FP EUDAMEDFDA UDI
- Description
- LED 150FP Lamp and suspension arm only (for use with a Kenex celling radiation shield) inclu PSU FDA UDI
Identifiers
- Catalog Number
- 300/L-LED150FP FDA UDI
- Primary DI / UDI-DI
- 05055449410397 EUDAMEDFDA UDI
- Basic UDI-DI
- 50554494LIMWK EUDAMED
- FDA Product Code
- KZF FDA UDI
- EMDN Code
- Z12010701 FIXED SCIALYTIC LAMPS EUDAMED
- GMDN Term
- Fixed examination/treatment room light FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 880.6320 FDA UDI
- Market of Registration
- Germany EUDAMED
- 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
Yes
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: Operating room light system
LED 150FP Lamp and suspension arm only (for use with a Kenex celling radiation … by Kenex (electro-Medical) Limited — Class I — MDR, FDA UDI — listed in…
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 50554494LIMWK | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Kenex (Electro-Medical) Limited
- EUDAMED SRN
- GB-MF-000009022
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED bb2d6cfa-e16e-4f07-87bd-398ffcdd0be4 61 fields · synced Jun 17, 2026
- FDA UDI d898c9f4-6611-4fa7-9016-e285dbe81307 34 fields · synced May 30, 2026