eudamed_udi
Primary ID: 05055982763592
Maxi Move (UDI 05055982763592)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Maxi Move - Primary ID 05055982763592
Device Regulatory Overview
The Maxi Move (Model/Catalog Number: KMCEXN-D-99) 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
- KMCEXN-D-99
- Product Code / EMDN
- V0805030102
- Device Name
- SARA FLEX
- Database Sync Date
- 2026-08-09 16:28:45
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 Move?
The registered manufacturer of record for Maxi Move is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for Maxi Move?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055982763592.
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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