nxt Bipolar Forceps (UDI Atlas Choice Low Profile Ultra Non-Stick Bipolar Forceps - Bayonet - Black / Bl)
Manufactured by adeor Medical AG
Device Regulatory Overview
The nxt Bipolar Forceps (Model/Catalog Number: Atlas Choice Low Profile Ultra Non-Stick Bipolar Forceps - Bayonet - Black / Bl) is a medical device manufactured by adeor Medical AG. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Atlas Choice Low Profile Ultra Non-Stick Bipolar Forceps - Bayonet - Black / Bl
- Product Code / EMDN
- GEI
- Device Name
- Database Sync Date
- 2026-08-09 09:17:38
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of nxt Bipolar Forceps?
The registered manufacturer of record for nxt Bipolar Forceps is adeor Medical AG.
What is the Primary UDI-DI identifier for nxt Bipolar Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Atlas Choice Low Profile Ultra Non-Stick Bipolar Forceps - Bayonet - Black / Bl.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Other Devices by adeor Medical AG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint