gudid
Primary ID: VM57-1161
Avalign (UDI VM57-1161)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Avalign - Primary ID VM57-1161
Device Regulatory Overview
The Avalign (Model/Catalog Number: VM57-1161) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification HDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VM57-1161
- Product Code / EMDN
- HDF
- Device Name
- Weisman Graves Vaginal Speculum, left open, medium, 100mm x 35mm
- Database Sync Date
- 2026-08-09 09:02:38
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 Avalign?
The registered manufacturer of record for Avalign is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for Avalign?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VM57-1161.
What classification code is assigned to this device?
This device is registered under product classification code HDF.
Similar Classification Devices (HDF)
Other Devices by Avalign Technologies, Inc.
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