eudamed_udi
Primary ID: 05051968035202
SONICAID (UDI 05051968035202)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SONICAID - Primary ID 05051968035202
Device Regulatory Overview
The SONICAID (Model/Catalog Number: TEAM3A B3) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification Z12080101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TEAM3A B3
- Product Code / EMDN
- Z12080101
- Device Name
- ANTEPARTUM/PRINTER
- Database Sync Date
- 2026-08-09 17:09:48
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 SONICAID?
The registered manufacturer of record for SONICAID is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for SONICAID?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051968035202.
What classification code is assigned to this device?
This device is registered under product classification code Z12080101.
Similar Classification Devices (Z12080101)
Other Devices by ArjoHuntleigh AB
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint