GUDIDData
eudamed_udi Primary ID: 06970385729497

Spacer For Aerosol (UDI 06970385729497)

Manufactured by Xiamen Tianzuo Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spacer For Aerosol - Primary ID 06970385729497

Device Regulatory Overview

The Spacer For Aerosol (Model/Catalog Number: SFA-VS-220ml) is a medical device manufactured by Xiamen Tianzuo Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SFA-VS-220ml
Product Code / EMDN
R03010302
Device Name
Spacer For Aerosol
Database Sync Date
2026-08-09 17:05:31

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 Spacer For Aerosol?

The registered manufacturer of record for Spacer For Aerosol is Xiamen Tianzuo Medical Co., Ltd..

What is the Primary UDI-DI identifier for Spacer For Aerosol?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970385729497.

What classification code is assigned to this device?

This device is registered under product classification code R03010302.

Programmatic Export

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

JSON API Endpoint