eudamed_udi
Primary ID: 05056097350769
Maxi 500 (UDI 05056097350769)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Maxi 500 - Primary ID 05056097350769
Device Regulatory Overview
The Maxi 500 (Model/Catalog Number: KM560300-EUUK) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification V0805030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KM560300-EUUK
- Product Code / EMDN
- V0805030102
- Device Name
- Tenor
- Database Sync Date
- 2026-08-09 16:29:58
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 Maxi 500?
The registered manufacturer of record for Maxi 500 is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for Maxi 500?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056097350769.
What classification code is assigned to this device?
This device is registered under product classification code V0805030102.
Similar Classification Devices (V0805030102)
Other Devices by ArjoHuntleigh AB
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