ATMOS (UDI HL 21 LED (examination set))
Manufactured by ATMOS MedizinTechnik GmbH & Co. KG
Device Regulatory Overview
The ATMOS (Model/Catalog Number: HL 21 LED (examination set)) is a medical device manufactured by ATMOS MedizinTechnik GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HL 21 LED (examination set)
- Product Code / EMDN
- KZF
- Device Name
- The product is a cold light source for medical use. The light source can be worn on the head and enables the illumination of the viewing area for diagnostic purposes.
- Database Sync Date
- 2026-08-09 09:11:39
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ATMOS?
The registered manufacturer of record for ATMOS is ATMOS MedizinTechnik GmbH & Co. KG.
What is the Primary UDI-DI identifier for ATMOS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HL 21 LED (examination set).
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
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