GUDIDData
eudamed_udi Primary ID: 08906030752846

Mucus Extractor (UDI 08906030752846)

Manufactured by Lars Medicare Pvt Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mucus Extractor - Primary ID 08906030752846

Device Regulatory Overview

The Mucus Extractor (Model/Catalog Number: 15250.00) is a medical device manufactured by Lars Medicare Pvt Ltd. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
15250.00
Product Code / EMDN
R05010301
Device Name
Mucus Extractor
Database Sync Date
2026-08-09 16:46:10

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 Mucus Extractor?

The registered manufacturer of record for Mucus Extractor is Lars Medicare Pvt Ltd.

What is the Primary UDI-DI identifier for Mucus Extractor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906030752846.

What classification code is assigned to this device?

This device is registered under product classification code R05010301.

Programmatic Export

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

JSON API Endpoint