eudamed_udi
Primary ID: 05600494148605
ISA™ XPLUS (UDI 05600494148605)
Manufactured by Invacare Portugal, Unipessoal Lda.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ISA™ XPLUS - Primary ID 05600494148605
Device Regulatory Overview
The ISA™ XPLUS (Model/Catalog Number: 1682765) is a medical device manufactured by Invacare Portugal, Unipessoal Lda.. This product is indexed under FDA Product Code / Category Classification V0805030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1682765
- Product Code / EMDN
- V0805030102
- Device Name
- ISA
- Database Sync Date
- 2026-08-09 16:29:04
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 ISA™ XPLUS?
The registered manufacturer of record for ISA™ XPLUS is Invacare Portugal, Unipessoal Lda..
What is the Primary UDI-DI identifier for ISA™ XPLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600494148605.
What classification code is assigned to this device?
This device is registered under product classification code V0805030102.
Similar Classification Devices (V0805030102)
Other Devices by Invacare Portugal, Unipessoal Lda.
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