LINEA GGDF 30 SILK TOE COD. EU071 MIS. UNICA CONF. DA 3 PZ ITA/ENG (UDI 08056598550160)
Manufactured by EUMEDICA SRL
Device Regulatory Overview
The LINEA GGDF 30 SILK TOE COD. EU071 MIS. UNICA CONF. DA 3 PZ ITA/ENG (Model/Catalog Number: EU071) 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
- EU071
- Product Code / EMDN
- M03030299
- Device Name
- LINEA GGDF30 LUXURY
- Database Sync Date
- 2026-08-09 16:29:14
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 LINEA GGDF 30 SILK TOE COD. EU071 MIS. UNICA CONF. DA 3 PZ ITA/ENG?
The registered manufacturer of record for LINEA GGDF 30 SILK TOE COD. EU071 MIS. UNICA CONF. DA 3 PZ ITA/ENG is EUMEDICA SRL.
What is the Primary UDI-DI identifier for LINEA GGDF 30 SILK TOE COD. EU071 MIS. UNICA CONF. DA 3 PZ ITA/ENG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056598550160.
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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