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NIM Eclipse

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
NIM Eclipse FDA UDI
Generic Name
Nerve-locating system FDA UDI
Device Name
MODULE 945OPM660LO LOANER PATIENT FDA UDI
Model / Reference
945OPM660LO FDA UDI
Description
MODULE 945OPM660LO LOANER PATIENT FDA UDI

Identifiers

Primary DI / UDI-DI
00643169793880 FDA UDI
510(k) Number
K061639 FDA UDI
FDA Product Code
GWJ FDA UDI
ITX FDA UDI
GWE FDA UDI
GWF FDA UDI
IYN FDA UDI
GWQ FDA UDI
GMDN Term
Nerve-locating system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1900 FDA UDI
892.1570 FDA UDI
882.1890 FDA UDI
882.1870 FDA UDI
892.1550 FDA UDI
882.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nerve-locating system

NIM Eclipse by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nerve-locating system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 710366f4-5ade-4bc4-a7d2-f0ed285c9bcf 36 fields · synced May 30, 2026