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Keenhealth

FDA UDI

Class I (US FDA UDI)

by Sevenground Trading B.V.

Identity

Trade Name
Keenhealth FDA UDI
Generic Name
Nasal breathing aid, external FDA UDI
Device Name
K-NS-356 is a better breath Stop Snoring Nasal Strips FDA UDI
Model / Reference
K-NS-356-30 FDA UDI
Description
K-NS-356 is a better breath Stop Snoring Nasal Strips FDA UDI

Identifiers

Primary DI / UDI-DI
08719699632448 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Nasal breathing aid, external FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

No

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

No

FDA UDI

Category: Nasal breathing aid, external

Keenhealth by Sevenground Trading B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal breathing aid, external.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ede3266-33ae-45a8-8db8-1ccf7c5be04a 34 fields · synced May 30, 2026