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VentStar humidifier chamber (N)

FDA UDI

Class II (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
VentStar humidifier chamber (N) FDA UDI
Generic Name
Inspiratory line humidification chamber, single-use FDA UDI
Model / Reference
MP02590 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675389583 FDA UDI
510(k) Number
K222822 FDA UDI
FDA Product Code
BZE FDA UDI
GMDN Term
Inspiratory line humidification chamber, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5270 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Inspiratory line humidification chamber, single-use

VentStar humidifier chamber (N) by Drägerwerk AG & Co. KGaA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inspiratory line humidification chamber, single-use.

Cleared under the same submission

K222822 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drägerwerk AG & Co. KGaA

Sources (1)

  • FDA UDI 39ca230e-6502-4a69-827f-e010e029d8e9 33 fields · synced Jun 1, 2026