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Nox A1 Carry Case

FDA UDI

Class II (US FDA UDI)

by Nox Medical ehf.

Identity

Trade Name
Nox A1 Carry Case FDA UDI
Generic Name
Polysomnograph FDA UDI
Model / Reference
NOX-A1_CC FDA UDI

Identifiers

Catalog Number
568011 FDA UDI
Primary DI / UDI-DI
15694311110095 FDA UDI
510(k) Number
K192469 FDA UDI
FDA Product Code
KZM FDA UDI
OLZ FDA UDI
GMDN Term
Polysomnograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1375 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polysomnograph

Nox A1 Carry Case by Nox Medical ehf. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polysomnograph.

Cleared under the same submission

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 b7fc9385-1736-4af9-8deb-4056e5de7b99 35 fields · synced May 31, 2026