eudamed_udi
Primary ID: 07611600832477
Arm sling (UDI 07611600832477)
Manufactured by IVF HARTMANN AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Arm sling - Primary ID 07611600832477
Device Regulatory Overview
The Arm sling (Model/Catalog Number: 832470) 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
- 832470
- Product Code / EMDN
- M030599
- Device Name
- Armtraggurt
- Database Sync Date
- 2026-08-09 16:51:34
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 Arm sling?
The registered manufacturer of record for Arm sling is IVF HARTMANN AG.
What is the Primary UDI-DI identifier for Arm sling?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611600832477.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint