GUDIDData
eudamed_udi Primary ID: 08906065488789

Yankur Suction Set™ (UDI 08906065488789)

Manufactured by Mais India Medical Devices Pvt. Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Yankur Suction Set™ - Primary ID 08906065488789

Device Regulatory Overview

The Yankur Suction Set™ (Model/Catalog Number: MI/CA/01-000-E) is a medical device manufactured by Mais India Medical Devices Pvt. Ltd.. This product is indexed under FDA Product Code / Category Classification Z12159009 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MI/CA/01-000-E
Product Code / EMDN
Z12159009
Device Name
Yankauer Handle with Connecting Tube
Database Sync Date
2026-08-09 17:26:33

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 Yankur Suction Set™?

The registered manufacturer of record for Yankur Suction Set™ is Mais India Medical Devices Pvt. Ltd..

What is the Primary UDI-DI identifier for Yankur Suction Set™?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906065488789.

What classification code is assigned to this device?

This device is registered under product classification code Z12159009.

Programmatic Export

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

JSON API Endpoint