gudid
Primary ID: 2000.0003
debritom+ (UDI 2000.0003)
Manufactured by Medaxis AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for debritom+ - Primary ID 2000.0003
Device Regulatory Overview
The debritom+ (Model/Catalog Number: 2000.0003) is a medical device manufactured by Medaxis AG. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2000.0003
- Product Code / EMDN
- FQH
- Device Name
- debritom+ handpiece standard jet
- Database Sync Date
- 2026-08-09 09:06:29
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 debritom+?
The registered manufacturer of record for debritom+ is Medaxis AG.
What is the Primary UDI-DI identifier for debritom+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2000.0003.
What classification code is assigned to this device?
This device is registered under product classification code FQH.
Similar Classification Devices (FQH)
Other Devices by Medaxis AG
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