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Unimed

FDA UDI

Class II (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name
Unimed FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
Disposable blood oxygen probe/adhesive foam /Masimo/RD Rainbow Set/adult /0.9M FDA UDI
Model / Reference
F503-254R FDA UDI
Description
Disposable blood oxygen probe/adhesive foam /Masimo/RD Rainbow Set/adult /0.9M FDA UDI

Identifiers

Primary DI / UDI-DI
06945664899130 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter probe, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulse oximeter probe, single-use

Unimed by Unimed Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e928970e-1006-4fc3-9a7c-50aced97a51a 33 fields · synced Jun 1, 2026