Phytosun Aroms Toux enfant seche e grasse (UDI 04251778111252)
Manufactured by HÄLSA Pharma GmbH
Device Regulatory Overview
The Phytosun Aroms Toux enfant seche e grasse (Model/Catalog Number: 9531890) is a medical device manufactured by HÄLSA Pharma GmbH. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9531890
- Product Code / EMDN
- Q030199
- Device Name
- MD Marshmallow
- Database Sync Date
- 2026-08-09 17:04:00
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 Phytosun Aroms Toux enfant seche e grasse?
The registered manufacturer of record for Phytosun Aroms Toux enfant seche e grasse is HÄLSA Pharma GmbH.
What is the Primary UDI-DI identifier for Phytosun Aroms Toux enfant seche e grasse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251778111252.
What classification code is assigned to this device?
This device is registered under product classification code Q030199.
Similar Classification Devices (Q030199)
Other Devices by HÄLSA Pharma GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint