Sala-Med Vesemelegítő XL (UDI 05999571440344)
Manufactured by Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.
Device Regulatory Overview
The Sala-Med Vesemelegítő XL (Model/Catalog Number: 05999571440344) is a medical device manufactured by Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.. This product is indexed under FDA Product Code / Category Classification Y060399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 05999571440344
- Product Code / EMDN
- Y060399
- Device Name
- Sala-Med Vesemelegítő
- Database Sync Date
- 2026-08-09 17:07:27
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 Sala-Med Vesemelegítő XL?
The registered manufacturer of record for Sala-Med Vesemelegítő XL is Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft..
What is the Primary UDI-DI identifier for Sala-Med Vesemelegítő XL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05999571440344.
What classification code is assigned to this device?
This device is registered under product classification code Y060399.
Similar Classification Devices (Y060399)
Other Devices by Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.
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