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Oxygen Sensor

FDA UDI

Class II (US FDA UDI)

by Honeywell Healthcare Solutions GmbH

Identity

Trade Name
Oxygen Sensor FDA UDI
Generic Name
Respiratory oxygen sensor FDA UDI
Device Name
Oxygen Sensor OOMLF202-2R / REF 27990 FDA UDI
Model / Reference
OOMLF202-2R FDA UDI
Description
Oxygen Sensor OOMLF202-2R / REF 27990 FDA UDI

Identifiers

Catalog Number
E1002607 FDA UDI
Primary DI / UDI-DI
04036616010979 FDA UDI
510(k) Number
K082655 FDA UDI
FDA Product Code
CCL FDA UDI
GMDN Term
Respiratory oxygen sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1720 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

Yes

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

Dimensions & Sizes

Size
Length — 28 Millimeter FDA UDI
Width — 29 Millimeter FDA UDI
Weight — 23 Gram FDA UDI

Category: Respiratory oxygen sensor

Oxygen Sensor by Honeywell Healthcare Solutions GmbH — 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

Sources (1)

  • FDA UDI 0d228941-0d27-4824-b47b-932fdac3a240 38 fields · synced May 30, 2026