eudamed_udi
Primary ID: 08056598551792
EU-INSOLE S021F MIS. UNICA SX - CONF. DA 6 PZ (UDI 08056598551792)
Manufactured by EUMEDICA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EU-INSOLE S021F MIS. UNICA SX - CONF. DA 6 PZ - Primary ID 08056598551792
Device Regulatory Overview
The EU-INSOLE S021F MIS. UNICA SX - CONF. DA 6 PZ (Model/Catalog Number: S021SRF) is a medical device manufactured by EUMEDICA SRL. This product is indexed under FDA Product Code / Category Classification M03030299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S021SRF
- Product Code / EMDN
- M03030299
- Device Name
- DISPOSITIVI PIEDE
- Database Sync Date
- 2026-08-09 16:50:11
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 EU-INSOLE S021F MIS. UNICA SX - CONF. DA 6 PZ?
The registered manufacturer of record for EU-INSOLE S021F MIS. UNICA SX - CONF. DA 6 PZ is EUMEDICA SRL.
What is the Primary UDI-DI identifier for EU-INSOLE S021F MIS. UNICA SX - CONF. DA 6 PZ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056598551792.
What classification code is assigned to this device?
This device is registered under product classification code M03030299.
Similar Classification Devices (M03030299)
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