gudid
Primary ID: D16236000
neoBLUE Radiometer (UDI D16236000)
Manufactured by Derungs Licht AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for neoBLUE Radiometer - Primary ID D16236000
Device Regulatory Overview
The neoBLUE Radiometer (Model/Catalog Number: D16236000) is a medical device manufactured by Derungs Licht AG. This product is indexed under FDA Product Code / Category Classification JJQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D16236000
- Product Code / EMDN
- JJQ
- Device Name
- Blue light radiometer: An instrument designed to measure the radiant flux (radiant power) in the spectral range of 400 to 500 nm(i.e., blue) during bilirubinemia treatment for newborns and infants
- Database Sync Date
- 2026-08-09 09:16:11
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of neoBLUE Radiometer?
The registered manufacturer of record for neoBLUE Radiometer is Derungs Licht AG.
What is the Primary UDI-DI identifier for neoBLUE Radiometer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D16236000.
What classification code is assigned to this device?
This device is registered under product classification code JJQ.
Similar Classification Devices (JJQ)
Other Devices by Derungs Licht AG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint