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Vivo 45 LS

FDA UDI

Class II (US FDA UDI)

by Breas Medical AB

Identity

Trade Name
Vivo 45 LS FDA UDI
Generic Name
Respiratory oxygen sensor FDA UDI
Device Name
FiO2 Sensor FDA UDI
Model / Reference
006172 FDA UDI
Description
FiO2 Sensor FDA UDI

Identifiers

Catalog Number
006172 FDA UDI
Primary DI / UDI-DI
07321820061723 FDA UDI
510(k) Number
K193586 FDA UDI
FDA Product Code
CBK FDA UDI
NOU FDA UDI
GMDN Term
Respiratory oxygen sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Respiratory oxygen sensor

Vivo 45 LS by Breas Medical AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory oxygen sensor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Breas Medical AB

Sources (1)

  • FDA UDI 80783101-3f46-4658-a786-1e812bac7285 36 fields · synced May 30, 2026