gudid
Primary ID: 90T2113
ZeroWire G2 (UDI 90T2113)
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 90T2113
Device Regulatory Overview
The ZeroWire G2 (Model/Catalog Number: 90T2113) 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
- 90T2113
- Product Code / EMDN
- GCJ
- Device Name
- DePuy Synthes, ZeroWire G2 Accessory Kit, Pair: Radiance Ultra 32
- 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 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 90T2113.
What classification code is assigned to this device?
This device is registered under product classification code GCJ.
Similar Classification Devices (GCJ)
Other Devices by Nds Surgical Imaging LLC
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