StimSite Activation Card

FDA UDI

Class II (US FDA UDI)

by Northgate Technologies Inc.

Identity

Trade Name: StimSite Activation Card FDA UDI
Generic Name: Nerve-locating system FDA UDI
Device Name: Activation Card, StimSite, Single FDA UDI
Model / Reference: AM-2101 FDA UDI
Description: Activation Card, StimSite, Single FDA UDI

Identifiers

Primary DI / UDI-DI: 00817183020776 FDA UDI
510(k) Number: K200886 FDA UDI
FDA Product Code: ETN FDA UDI
GMDN Term: Nerve-locating system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Nerve-locating system

StimSite Activation Card by Northgate Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Nerve-locating system.

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AVANOS — Avanos Medical, Inc. · Class II
NIM-ECLIPSE® — MEDTRONIC XOMED, INC. · Class II
NIM-Eclipse® — MEDTRONIC XOMED, INC. · Class II
SENTIO — Medos International Sàrl · Class II
Halyard — Avanos Medical, Inc. · Class II

Cleared under the same submission

K200886 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Northgate Technologies Inc.

Sources (1)

FDA UDI f2ba28a9-6fb0-4bac-b9e3-1c77502dd013 34 fields · synced Jun 6, 2026