GUDIDData
eudamed_udi Primary ID: 04066098487044

Carryline Mobil (UDI 04066098487044)

Manufactured by Greiner GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Carryline Mobil - Primary ID 04066098487044

Device Regulatory Overview

The Carryline Mobil (Model/Catalog Number: 4870200) is a medical device manufactured by Greiner GmbH. This product is indexed under FDA Product Code / Category Classification V080502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
4870200
Product Code / EMDN
V080502
Device Name
Carryline
Database Sync Date
2026-08-09 16:46:02

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 Carryline Mobil?

The registered manufacturer of record for Carryline Mobil is Greiner GmbH.

What is the Primary UDI-DI identifier for Carryline Mobil?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04066098487044.

What classification code is assigned to this device?

This device is registered under product classification code V080502.

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