eudamed_udi
Primary ID: 04251110628202
Rücklaufsperre (UDI 04251110628202)
Manufactured by ATO FORM GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rücklaufsperre - Primary ID 04251110628202
Device Regulatory Overview
The Rücklaufsperre (Model/Catalog Number: MGO-25346) is a medical device manufactured by ATO FORM GmbH. This product is indexed under FDA Product Code / Category Classification Y0580 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MGO-25346
- Product Code / EMDN
- Y0580
- Device Name
- Thoraxring Umfang 70 cm
- Database Sync Date
- 2026-08-09 17:41:37
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Rücklaufsperre?
The registered manufacturer of record for Rücklaufsperre is ATO FORM GmbH.
What is the Primary UDI-DI identifier for Rücklaufsperre?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251110628202.
What classification code is assigned to this device?
This device is registered under product classification code Y0580.
Similar Classification Devices (Y0580)
Other Devices by ATO FORM GmbH
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