GUDIDData
eudamed_udi Primary ID: 08058756046331

DOUBLE MEDI FORM SD RIV. BIOCERAMICA MIMOSA TRAPUNTATO 165X190 (UDI 08058756046331)

Manufactured by Frassiflex Srl

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DOUBLE MEDI FORM SD RIV. BIOCERAMICA MIMOSA TRAPUNTATO 165X190 - Primary ID 08058756046331

Device Regulatory Overview

The DOUBLE MEDI FORM SD RIV. BIOCERAMICA MIMOSA TRAPUNTATO 165X190 (Model/Catalog Number: FDMb060Sr06816519023) is a medical device manufactured by Frassiflex Srl. This product is indexed under FDA Product Code / Category Classification V0899 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FDMb060Sr06816519023
Product Code / EMDN
V0899
Device Name
Materassi Schiumato
Database Sync Date
2026-08-09 16:28:44

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of DOUBLE MEDI FORM SD RIV. BIOCERAMICA MIMOSA TRAPUNTATO 165X190?

The registered manufacturer of record for DOUBLE MEDI FORM SD RIV. BIOCERAMICA MIMOSA TRAPUNTATO 165X190 is Frassiflex Srl.

What is the Primary UDI-DI identifier for DOUBLE MEDI FORM SD RIV. BIOCERAMICA MIMOSA TRAPUNTATO 165X190?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058756046331.

What classification code is assigned to this device?

This device is registered under product classification code V0899.

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