GUDIDData
eudamed_udi Primary ID: 04056719000868

BlueBAG BodyFIX 14 T-Shape 1130x1375 mm/51L (UDI 04056719000868)

Manufactured by 3C-Medical Intelligence GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BlueBAG BodyFIX 14 T-Shape 1130x1375 mm/51L - Primary ID 04056719000868

Device Regulatory Overview

The BlueBAG BodyFIX 14 T-Shape 1130x1375 mm/51L (Model/Catalog Number: P10104-836) is a medical device manufactured by 3C-Medical Intelligence GmbH. This product is indexed under FDA Product Code / Category Classification V0804 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
P10104-836
Product Code / EMDN
V0804
Device Name
BodyFIX, BlueBAG
Database Sync Date
2026-08-09 16:44:58

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 BlueBAG BodyFIX 14 T-Shape 1130x1375 mm/51L?

The registered manufacturer of record for BlueBAG BodyFIX 14 T-Shape 1130x1375 mm/51L is 3C-Medical Intelligence GmbH.

What is the Primary UDI-DI identifier for BlueBAG BodyFIX 14 T-Shape 1130x1375 mm/51L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056719000868.

What classification code is assigned to this device?

This device is registered under product classification code V0804.

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