eudamed_udi
Primary ID: 42700011211377
IO (UDI 42700011211377)
Manufactured by Mosler Stuntebeck Müller GbR
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IO - Primary ID 42700011211377
Device Regulatory Overview
The IO (Model/Catalog Number: IO_01_137CM_L) is a medical device manufactured by Mosler Stuntebeck Müller GbR. This product is indexed under FDA Product Code / Category Classification Y120303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IO_01_137CM_L
- Product Code / EMDN
- Y120303
- Device Name
- IO
- Database Sync Date
- 2026-08-09 16:51:52
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 IO?
The registered manufacturer of record for IO is Mosler Stuntebeck Müller GbR.
What is the Primary UDI-DI identifier for IO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42700011211377.
What classification code is assigned to this device?
This device is registered under product classification code Y120303.
Similar Classification Devices (Y120303)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint