GUDIDData
eudamed_udi Primary ID: 06979166920023

Canister (UDI 06979166920023)

Manufactured by Shijiazhuang Yuanding Medical Device Co.,LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Canister - Primary ID 06979166920023

Device Regulatory Overview

The Canister (Model/Catalog Number: YDPA35) is a medical device manufactured by Shijiazhuang Yuanding Medical Device Co.,LTD. This product is indexed under FDA Product Code / Category Classification A0680 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
YDPA35
Product Code / EMDN
A0680
Device Name
Canister
Database Sync Date
2026-08-09 17:49:33

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 Canister?

The registered manufacturer of record for Canister is Shijiazhuang Yuanding Medical Device Co.,LTD.

What is the Primary UDI-DI identifier for Canister?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06979166920023.

What classification code is assigned to this device?

This device is registered under product classification code A0680.

Programmatic Export

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

JSON API Endpoint