eudamed_udi
Primary ID: 05051986006826
235mm Allis (UDI 05051986006826)
Manufactured by Surgical Innovations Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 235mm Allis - Primary ID 05051986006826
Device Regulatory Overview
The 235mm Allis (Model/Catalog Number: 101-47028) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification L180802 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101-47028
- Product Code / EMDN
- L180802
- Device Name
- 235mm Allis
- Database Sync Date
- 2026-08-09 16:45:41
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 235mm Allis?
The registered manufacturer of record for 235mm Allis is Surgical Innovations Ltd..
What is the Primary UDI-DI identifier for 235mm Allis?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986006826.
What classification code is assigned to this device?
This device is registered under product classification code L180802.
Similar Classification Devices (L180802)
Other Devices by Surgical Innovations Ltd.
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