Allengers (UDI 08904139700348)
Manufactured by Allengers Medical Systems Limited
Device Regulatory Overview
The Allengers (Model/Catalog Number: AMSL/UM/MARS 20DR/XX/27) is a medical device manufactured by Allengers Medical Systems Limited. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AMSL/UM/MARS 20DR/XX/27
- Product Code / EMDN
- Z11039016
- Device Name
- High Frequency X-Ray Machine (with Radiography, Radiography/Fluoroscopy, Digital Radiography)
- Database Sync Date
- 2026-08-09 16:49:00
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 Allengers?
The registered manufacturer of record for Allengers is Allengers Medical Systems Limited.
What is the Primary UDI-DI identifier for Allengers?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08904139700348.
What classification code is assigned to this device?
This device is registered under product classification code Z11039016.
Similar Classification Devices (Z11039016)
Other Devices by Allengers Medical Systems Limited
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