eudamed_udi
Primary ID: 00990010301627
Airlight (UDI 00990010301627)
Manufactured by Beyes Dental Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Airlight - Primary ID 00990010301627
Device Regulatory Overview
The Airlight (Model/Catalog Number: HP6018P) is a medical device manufactured by Beyes Dental Inc. This product is indexed under FDA Product Code / Category Classification Z12119099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HP6018P
- Product Code / EMDN
- Z12119099
- Device Name
- M800P-M/PD
- Database Sync Date
- 2026-08-09 16:45:06
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 Airlight?
The registered manufacturer of record for Airlight is Beyes Dental Inc.
What is the Primary UDI-DI identifier for Airlight?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00990010301627.
What classification code is assigned to this device?
This device is registered under product classification code Z12119099.
Similar Classification Devices (Z12119099)
Other Devices by Beyes Dental Inc
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