GUDIDData
gudid Primary ID: 90Z178

ZeroWire G2 (UDI 90Z178)

Manufactured by Nds Surgical Imaging LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZeroWire G2 - Primary ID 90Z178

Device Regulatory Overview

The ZeroWire G2 (Model/Catalog Number: 90Z178) is a medical device manufactured by Nds Surgical Imaging LLC. This product is indexed under FDA Product Code / Category Classification GCJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
90Z178
Product Code / EMDN
GCJ
Device Name
ZeroWire G2 Duo Accessory Kit, Radiance Ultra 32" / EndoVue 32"
Database Sync Date
2026-08-09 09:32:54

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of ZeroWire G2?

The registered manufacturer of record for ZeroWire G2 is Nds Surgical Imaging LLC.

What is the Primary UDI-DI identifier for ZeroWire G2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90Z178.

What classification code is assigned to this device?

This device is registered under product classification code GCJ.

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