gudid
Primary ID: 10-320117
IMS (UDI 10-320117)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IMS - Primary ID 10-320117
Device Regulatory Overview
The IMS (Model/Catalog Number: 10-320117) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification DXC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-320117
- Product Code / EMDN
- DXC
- Device Name
- Cooley Vascular Tissue Forceps, TW 2.0mm OL 195mm(7 5/8")
- Database Sync Date
- 2026-08-09 09:02:35
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 IMS?
The registered manufacturer of record for IMS is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for IMS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-320117.
What classification code is assigned to this device?
This device is registered under product classification code DXC.
Similar Classification Devices (DXC)
Other Devices by Avalign Technologies, Inc.
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