gudid
Primary ID: 439, 438, 413
Avivatens Pain Management (UDI 439, 438, 413)
Manufactured by BIO-MEDICAL RESEARCH LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Avivatens Pain Management - Primary ID 439, 438, 413
Device Regulatory Overview
The Avivatens Pain Management (Model/Catalog Number: 439, 438, 413) is a medical device manufactured by BIO-MEDICAL RESEARCH LIMITED. This product is indexed under FDA Product Code / Category Classification NYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 439, 438, 413
- Product Code / EMDN
- NYN
- Device Name
- Database Sync Date
- 2026-08-09 09:22:51
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 Avivatens Pain Management?
The registered manufacturer of record for Avivatens Pain Management is BIO-MEDICAL RESEARCH LIMITED.
What is the Primary UDI-DI identifier for Avivatens Pain Management?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 439, 438, 413.
What classification code is assigned to this device?
This device is registered under product classification code NYN.
Similar Classification Devices (NYN)
Other Devices by BIO-MEDICAL RESEARCH LIMITED
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