gudid
Primary ID: 90K0086
EndoVue (UDI 90K0086)
Manufactured by Nds Surgical Imaging LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EndoVue - Primary ID 90K0086
Device Regulatory Overview
The EndoVue (Model/Catalog Number: 90K0086) is a medical device manufactured by Nds Surgical Imaging LLC. This product is indexed under FDA Product Code / Category Classification KQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90K0086
- Product Code / EMDN
- KQM
- Device Name
- ENDOVUE PLUS 24" (2018 Series) BC-WU24-A1417
- Database Sync Date
- 2026-08-09 09:32:54
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 EndoVue?
The registered manufacturer of record for EndoVue is Nds Surgical Imaging LLC.
What is the Primary UDI-DI identifier for EndoVue?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90K0086.
What classification code is assigned to this device?
This device is registered under product classification code KQM.
Similar Classification Devices (KQM)
Other Devices by Nds Surgical Imaging LLC
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