eudamed_udi
Primary ID: 07611600832415
Armtraggurt (UDI 07611600832415)
Manufactured by IVF HARTMANN AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Armtraggurt - Primary ID 07611600832415
Device Regulatory Overview
The Armtraggurt (Model/Catalog Number: 832410) is a medical device manufactured by IVF HARTMANN AG. This product is indexed under FDA Product Code / Category Classification M030599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 832410
- Product Code / EMDN
- M030599
- Device Name
- Armtraggurt
- Database Sync Date
- 2026-08-09 18:41:52
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 Armtraggurt?
The registered manufacturer of record for Armtraggurt is IVF HARTMANN AG.
What is the Primary UDI-DI identifier for Armtraggurt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611600832415.
What classification code is assigned to this device?
This device is registered under product classification code M030599.
Similar Classification Devices (M030599)
Other Devices by IVF HARTMANN AG
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