gudid
Primary ID: HL 21 LED
ATMOS (UDI HL 21 LED)
Manufactured by ATMOS MedizinTechnik GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ATMOS - Primary ID HL 21 LED
Device Regulatory Overview
The ATMOS (Model/Catalog Number: HL 21 LED) 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
- 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.
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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