GUDIDData
eudamed_udi Primary ID: 14062183071508

DEHP (UDI 14062183071508)

Manufactured by CB Healthcare Consulting GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DEHP - Primary ID 14062183071508

Device Regulatory Overview

The DEHP (Model/Catalog Number: 9797098) is a medical device manufactured by CB Healthcare Consulting GmbH. This product is indexed under FDA Product Code / Category Classification S01010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
9797098
Product Code / EMDN
S01010101
Device Name
Sterilisation Packaging
Database Sync Date
2026-08-09 16:29:45

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of DEHP?

The registered manufacturer of record for DEHP is CB Healthcare Consulting GmbH.

What is the Primary UDI-DI identifier for DEHP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14062183071508.

What classification code is assigned to this device?

This device is registered under product classification code S01010101.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint