Identity

Trade Name
Nosiboo Pro FDA UDI
Generic Name
Nasal aspirator, vacuum FDA UDI
Device Name
Nosiboo Pro electric nasal aspirator, grey, US version FDA UDI
Model / Reference
NO-05-04 FDA UDI
Description
Nosiboo Pro electric nasal aspirator, grey, US version FDA UDI

Identifiers

Catalog Number
NO-05-04 FDA UDI
Primary DI / UDI-DI
05999861015740 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Nasal aspirator, vacuum FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal aspirator, vacuum

Nosiboo Pro by ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal aspirator, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3b781978-16fa-4ab4-885e-c075f06afe30 34 fields · synced Jun 8, 2026