eudamed_udi
Primary ID: 08055400671970
VITE SPONGIOSA Ø3MM L80MM ST (UDI 08055400671970)
Manufactured by Mikai s.p.a.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VITE SPONGIOSA Ø3MM L80MM ST - Primary ID 08055400671970
Device Regulatory Overview
The VITE SPONGIOSA Ø3MM L80MM ST (Model/Catalog Number: 5000207ST) is a medical device manufactured by Mikai s.p.a.. This product is indexed under FDA Product Code / Category Classification P09120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5000207ST
- Product Code / EMDN
- P09120602
- Device Name
- Acciaio
- Database Sync Date
- 2026-08-09 16:29:11
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 VITE SPONGIOSA Ø3MM L80MM ST?
The registered manufacturer of record for VITE SPONGIOSA Ø3MM L80MM ST is Mikai s.p.a..
What is the Primary UDI-DI identifier for VITE SPONGIOSA Ø3MM L80MM ST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055400671970.
What classification code is assigned to this device?
This device is registered under product classification code P09120602.
Similar Classification Devices (P09120602)
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