eudamed_udi
Primary ID: 05055982760454
Arjo (UDI 05055982760454)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Arjo - Primary ID 05055982760454
Device Regulatory Overview
The Arjo (Model/Catalog Number: 700-19420) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification V0805038001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 700-19420
- Product Code / EMDN
- V0805038001
- Device Name
- Spreader Bar
- Database Sync Date
- 2026-08-09 16:29:07
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 Arjo?
The registered manufacturer of record for Arjo is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for Arjo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055982760454.
What classification code is assigned to this device?
This device is registered under product classification code V0805038001.
Similar Classification Devices (V0805038001)
Other Devices by ArjoHuntleigh AB
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