Neonav® ECG Adapter

FDA UDI

Class II (US FDA UDI)

by Navi Medical Technologies

Identity

Trade Name: Neonav® ECG Adapter FDA UDI
Generic Name: Electrocardiographic lead/catheter adaptor FDA UDI
Model / Reference: NV1-CN-ADP FDA UDI

Identifiers

Catalog Number: NV1-CN-ADP FDA UDI
Primary DI / UDI-DI: 09369999358679 FDA UDI
510(k) Number: K241910 FDA UDI
FDA Product Code: LJS FDA UDI
GMDN Term: Electrocardiographic lead/catheter adaptor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5970 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Electrocardiographic lead/catheter adaptor

Neonav® ECG Adapter by Navi Medical Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Electrocardiographic lead/catheter adaptor.

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Cleared under the same submission

K241910 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: Navi Medical Technologies

Sources (1)

FDA UDI 94919775-6f77-4c02-9e40-908cfbaab541 34 fields · synced Jun 8, 2026