eudamed_udi
Primary ID: 05600166943958
COGWEB (UDI 05600166943958)
Manufactured by NEUROINOVA, LDA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COGWEB - Primary ID 05600166943958
Device Regulatory Overview
The COGWEB (Model/Catalog Number: COG.PRO.02) is a medical device manufactured by NEUROINOVA, LDA. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- COG.PRO.02
- Product Code / EMDN
- V92
- Device Name
- COGWEB
- Database Sync Date
- 2026-08-09 16:30:31
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 COGWEB?
The registered manufacturer of record for COGWEB is NEUROINOVA, LDA.
What is the Primary UDI-DI identifier for COGWEB?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600166943958.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
Other Devices by NEUROINOVA, LDA
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