eudamed_udi Primary ID: 06975700084664

Stoma Paste (UDI 06975700084664)

Manufactured by Concarey Medical Technology Co., Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Stoma Paste (Model/Catalog Number: 12051) is a medical device manufactured by Concarey Medical Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification A108002,A108008 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 12051
Product Code / EMDN: A108002,A108008
Device Name: Stoma Paste
Database Sync Date: 2026-08-09 19:05:18

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 Stoma Paste?

The registered manufacturer of record for Stoma Paste is Concarey Medical Technology Co., Ltd.

What is the Primary UDI-DI identifier for Stoma Paste?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975700084664.

What classification code is assigned to this device?

This device is registered under product classification code A108002,A108008.

Other Devices by Concarey Medical Technology Co., Ltd

Programmatic Export

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

JSON API Endpoint