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Easy@Home Fingertip Pulse Oximeter

FDA UDI

Class II (US FDA UDI)

by Easy Healthcare Corporation

Identity

Trade Name
Easy@Home Fingertip Pulse Oximeter FDA UDI
Generic Name
Telemetric pulse oximeter FDA UDI
Model / Reference
EHP50D1 FDA UDI

Identifiers

Primary DI / UDI-DI
00850253007116 FDA UDI
510(k) Number
K082641 FDA UDI
FDA Product Code
OCH FDA UDI
GMDN Term
Telemetric 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Telemetric pulse oximeter

Easy@Home Fingertip Pulse Oximeter by Easy Healthcare Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Telemetric pulse oximeter.

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 3eeab0d5-7117-406c-985f-1c863889da82 33 fields · synced May 30, 2026