GUDIDData
eudamed_udi Primary ID: 08907265011166

AERO MIST (UDI 08907265011166)

Manufactured by Romsons Group Private Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AERO MIST - Primary ID 08907265011166

Device Regulatory Overview

The AERO MIST (Model/Catalog Number: SH-2074S KAD) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification R03010304 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SH-2074S KAD
Product Code / EMDN
R03010304
Device Name
NEBULIZER: Mask / Mouth Piece with Nebulization Chamber and Tubing.
Database Sync Date
2026-08-09 16:47:25

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of AERO MIST?

The registered manufacturer of record for AERO MIST is Romsons Group Private Limited.

What is the Primary UDI-DI identifier for AERO MIST?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265011166.

What classification code is assigned to this device?

This device is registered under product classification code R03010304.

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