eudamed_udi
Primary ID: 04057532600624
Spinova Mum, Sz.2 (UDI 04057532600624)
Manufactured by Bauerfeind AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spinova Mum, Sz.2 - Primary ID 04057532600624
Device Regulatory Overview
The Spinova Mum, Sz.2 (Model/Catalog Number: 12285791000002) is a medical device manufactured by Bauerfeind AG. This product is indexed under FDA Product Code / Category Classification Y060303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12285791000002
- Product Code / EMDN
- Y060303
- Device Name
- Spinova Mum
- Database Sync Date
- 2026-08-09 18:29:03
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 Spinova Mum, Sz.2?
The registered manufacturer of record for Spinova Mum, Sz.2 is Bauerfeind AG.
What is the Primary UDI-DI identifier for Spinova Mum, Sz.2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04057532600624.
What classification code is assigned to this device?
This device is registered under product classification code Y060303.
Similar Classification Devices (Y060303)
Other Devices by Bauerfeind AG
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