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Nox SAS Body Cable - Left

FDA UDIEUDAMED

Class II (US FDA UDI)

by Nox Medical ehf.

Identity

Trade Name
Nox SAS Body Cable - Left FDA UDI
Generic Name
Analytical non-scalp cutaneous lead FDA UDI
Model / Reference
ESNAP4SASLMPAC1US FDA UDI

Identifiers

Catalog Number
562217 FDA UDI
Primary DI / UDI-DI
15694311111689 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Analytical non-scalp cutaneous lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Analytical non-scalp cutaneous lead

Nox SAS Body Cable - Left by Nox Medical ehf. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous lead.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nox Medical ehf.

Sources (2)

  • FDA UDI aabf1dfb-7e89-41cc-b91f-dd24c002718a 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026