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Nox RIP Starter Kit E, M

FDA UDI

Class I (US FDA UDI)

by Nox Medical ehf.

Identity

Trade Name
Nox RIP Starter Kit E, M FDA UDI
Generic Name
Polysomnograph FDA UDI
Model / Reference
NOX-EMBA1KIT2 FDA UDI

Identifiers

Catalog Number
558011 FDA UDI
Primary DI / UDI-DI
15694311110651 FDA UDI
FDA Product Code
CAT FDA UDI
MNR FDA UDI
GMDN Term
Polysomnograph FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 FDA UDI
868.2375 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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

Nox RIP Starter Kit E, M by Nox Medical ehf. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nox Medical ehf.

Sources (1)

  • FDA UDI decbb0ee-6530-493e-91df-b903083f2ca8 36 fields · synced May 31, 2026