eudamed_udi
Primary ID: 06975700080918
Stoma Paste (UDI 06975700080918)
Manufactured by Concarey Medical Technology Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Stoma Paste - Primary ID 06975700080918
Device Regulatory Overview
The Stoma Paste (Model/Catalog Number: 1301) is a medical device manufactured by Concarey Medical Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification A108002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1301
- Product Code / EMDN
- A108002
- Device Name
- Stoma Paste
- Database Sync Date
- 2026-08-09 18:46:21
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 06975700080918.
What classification code is assigned to this device?
This device is registered under product classification code A108002.
Similar Classification Devices (A108002)
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