eudamed_udi Primary ID: 08050999410375

BENDE DI GARZA CAMBRIC MT. 10 X 10 CM. (UDI 08050999410375)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BENDE DI GARZA CAMBRIC MT. 10 X 10 CM. (Model/Catalog Number: BG22) is a medical device manufactured by SA.VE.PA. SRL. This product is indexed under FDA Product Code / Category Classification M030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BG22
Product Code / EMDN: M030101
Device Name: Dispositivi per bendaggio e medicazione
Database Sync Date: 2026-08-09 16:30:41

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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Frequently Asked Questions

Who is the primary manufacturer of BENDE DI GARZA CAMBRIC MT. 10 X 10 CM.?

The registered manufacturer of record for BENDE DI GARZA CAMBRIC MT. 10 X 10 CM. is SA.VE.PA. SRL.

What is the Primary UDI-DI identifier for BENDE DI GARZA CAMBRIC MT. 10 X 10 CM.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050999410375.

What classification code is assigned to this device?

This device is registered under product classification code M030101.

Similar Classification Devices (M030101)

Other Devices by SA.VE.PA. SRL

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