eudamed_udi
Primary ID: 19349285000243
Aquamax (UDI 19349285000243)
Manufactured by NorrDia Belgium bv
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aquamax - Primary ID 19349285000243
Device Regulatory Overview
The Aquamax (Model/Catalog Number: HF03) is a medical device manufactured by NorrDia Belgium bv. This product is indexed under FDA Product Code / Category Classification F01060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HF03
- Product Code / EMDN
- F01060103
- Device Name
- Aquamax
- Database Sync Date
- 2026-08-09 16:48:43
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 Aquamax?
The registered manufacturer of record for Aquamax is NorrDia Belgium bv.
What is the Primary UDI-DI identifier for Aquamax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 19349285000243.
What classification code is assigned to this device?
This device is registered under product classification code F01060103.
Similar Classification Devices (F01060103)
Other Devices by NorrDia Belgium bv
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