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OxiVenT™ Sensor

FDA UDI

Class II (US FDA UDI)

by Sentec, Inc.

Identity

Trade Name
OxiVenT™ Sensor FDA UDI
Generic Name
Transcutaneous blood gas monitoring system FDA UDI
Device Name
Digital Sensor for non-invasive and continuous measurement of transcutaneous carbon dioxide and oxygen partial pressure as well as pulse oximetry. Suitable for adult, pediatric and neonatal patients. FDA UDI
Model / Reference
OV-A/P/N FDA UDI
Description
Digital Sensor for non-invasive and continuous measurement of transcutaneous carbon dioxide and oxygen partial pressure as well as pulse oximetry. Suitable for adult, pediatric and neonatal patients. FDA UDI

Identifiers

Primary DI / UDI-DI
07640121880742 FDA UDI
510(k) Number
K041548 FDA UDI
K071672 FDA UDI
K101690 FDA UDI
K151329 FDA UDI
FDA Product Code
DPZ FDA UDI
DQA FDA UDI
KLK FDA UDI
LKD FDA UDI
LPP FDA UDI
GMDN Term
Transcutaneous blood gas monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2710 FDA UDI
870.2700 FDA UDI
868.2500 FDA UDI
868.2480 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: Pulse Co-oximeter probe, reusableTranscutaneous blood gas monitor sensorTranscutaneous blood gas monitoring system

OxiVenT™ Sensor by Sentec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous blood gas monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sentec, Inc.

Sources (1)

  • FDA UDI 998105cb-f465-469a-98db-a9db1b810e6b 35 fields · synced May 30, 2026