Protekt Pulse

FDA UDI

Class II (US FDA UDI)

by Proactive Medical Products

Identity

Trade Name: Protekt Pulse FDA UDI
Generic Name: Pulse oximeter FDA UDI
Device Name: DELUXE RECHARGEABLE HANDHELD PULSE OXIMETER FDA UDI
Model / Reference: 20120 FDA UDI
Description: DELUXE RECHARGEABLE HANDHELD PULSE OXIMETER FDA UDI

Identifiers

Catalog Number: 20120 FDA UDI
Primary DI / UDI-DI: 05060488570308 FDA UDI
FDA Product Code: DQA FDA UDI
GMDN Term: Pulse oximeter 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Height — 1.5 Inch FDA UDI
Length — 3.5 Inch FDA UDI
Width — 6 Inch FDA UDI

Category: Pulse oximeter

Protekt Pulse by Proactive Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Pulse oximeter.

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ChoiceMMed — Beijing Choice Electronic Technology Co., Ltd. · Class II
ChoiceMMed — Beijing Choice Electronic Technology Co., Ltd. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Proactive Medical Products

Sources (1)

FDA UDI 0607a851-10df-44d9-b80a-c5df8e66c73d 36 fields · synced Jun 1, 2026