eudamed_udi Primary ID: 07350019596470

FERNO SPED II Ready2go Kit (UDI 07350019596470)

Manufactured by AB Germa

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FERNO SPED II Ready2go Kit (Model/Catalog Number: 23005001001) is a medical device manufactured by AB Germa. This product is indexed under FDA Product Code / Category Classification V0804 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 23005001001
Product Code / EMDN: V0804
Device Name: Vacuum Splints
Database Sync Date: 2026-08-09 16:29:01

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 FERNO SPED II Ready2go Kit?

The registered manufacturer of record for FERNO SPED II Ready2go Kit is AB Germa.

What is the Primary UDI-DI identifier for FERNO SPED II Ready2go Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350019596470.

What classification code is assigned to this device?

This device is registered under product classification code V0804.

Similar Classification Devices (V0804)

Other Devices by AB Germa

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