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AirTechniques

FDA UDI

Class I (US FDA UDI)

by Baldus Sedation GmbH & Co. KG

Identity

Trade Name
AirTechniques FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
To be used in nitrous-oxide-oxygen sedation systems. The Vacuum Control Block is a safety feature and is used to monitor and precisely adjust the vacuum/suction levels. FDA UDI
Model / Reference
NSP0020 FDA UDI
Description
To be used in nitrous-oxide-oxygen sedation systems. The Vacuum Control Block is a safety feature and is used to monitor and precisely adjust the vacuum/suction levels. FDA UDI

Identifiers

Primary DI / UDI-DI
04260635790684 FDA UDI
FDA Product Code
CAX FDA UDI
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2340 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

Yes

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: Ventilator breathing circuit, reusable

AirTechniques by Baldus Sedation GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8b9fdebc-a23d-499f-b51a-ecd9dbea37c6 33 fields · synced May 31, 2026