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Invent Medical

FDA UDI

Class II (US FDA UDI)

by Invent Medical Corporation

Identity

Trade Name
Invent Medical FDA UDI
Generic Name
Heated respiratory humidifier FDA UDI
Device Name
HFT150 Heated Respiratory Humidifier FDA UDI
Model / Reference
HFT150 FDA UDI
Description
HFT150 Heated Respiratory Humidifier FDA UDI

Identifiers

Primary DI / UDI-DI
00810055350209 FDA UDI
510(k) Number
K233707 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Heated respiratory humidifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5450 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Heated respiratory humidifier

Invent Medical by Invent Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heated respiratory humidifier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66c18121-8313-4138-ac20-13298aee9fcd 35 fields · synced May 30, 2026