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MediChoice

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
Pulse oximetry telemetric monitoring system transmitter FDA UDI
Device Name
Sensor Nellcor OxiMax SpO2 1.1 M, Boot Phillips Compatible, Reusable, Not Made with Natural Rubber Latex FDA UDI
Model / Reference
CL2307 FDA UDI
Description
Sensor Nellcor OxiMax SpO2 1.1 M, Boot Phillips Compatible, Reusable, Not Made with Natural Rubber Latex FDA UDI

Identifiers

Primary DI / UDI-DI
10885632060939 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximetry telemetric monitoring system transmitter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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
MRI Safety
MR Unsafe FDA UDI

Category: Pulse oximetry telemetric monitoring system transmitter

MediChoice by Owens & Minor Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximetry telemetric monitoring system transmitter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Owens & Minor Distribution, Inc.

Sources (1)

  • FDA UDI 9f20ee93-51ec-482a-b892-2d82a105412c 34 fields · synced Jun 8, 2026