← Back to catalogue

BUBBLE HUMIDIFIER 400cc

FDA UDI

Class I (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name
BUBBLE HUMIDIFIER 400cc FDA UDI
Generic Name
Room humidifier FDA UDI
Device Name
BUBBLE HUMIDIFIER 400cc FDA UDI
Model / Reference
HB-72600 FDA UDI
Description
BUBBLE HUMIDIFIER 400cc FDA UDI

Identifiers

Primary DI / UDI-DI
04716770726007 FDA UDI
FDA Product Code
KFZ FDA UDI
GMDN Term
Room humidifier FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5460 FDA UDI
Commercial Distribution
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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Room humidifier

BUBBLE HUMIDIFIER 400cc by Besmed Health Business Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Room humidifier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b1720338-d607-4445-a59c-b192f1713553 33 fields · synced May 30, 2026