eudamed_udi
Primary ID: 08436562860561
LUPA H.F 3D (UDI 08436562860561)
Manufactured by MIMSAL TRADE, S.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LUPA H.F 3D - Primary ID 08436562860561
Device Regulatory Overview
The LUPA H.F 3D (Model/Catalog Number: 09332-3) is a medical device manufactured by MIMSAL TRADE, S.L.. This product is indexed under FDA Product Code / Category Classification Z12040199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 09332-3
- Product Code / EMDN
- Z12040199
- Device Name
- LUPA
- Database Sync Date
- 2026-08-09 16:30:01
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 LUPA H.F 3D?
The registered manufacturer of record for LUPA H.F 3D is MIMSAL TRADE, S.L..
What is the Primary UDI-DI identifier for LUPA H.F 3D?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436562860561.
What classification code is assigned to this device?
This device is registered under product classification code Z12040199.
Similar Classification Devices (Z12040199)
Other Devices by MIMSAL TRADE, S.L.
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