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Dagamma

FDA UDI

Class II (US FDA UDI)

by Dagamma Inc.

Identity

Trade Name
Dagamma FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
The Dagamma DP-150 finger pulse oximeter is a lightweight, portable device used for measuring both heart rate and blood oxygen levels or SpO2. FDA UDI
Model / Reference
Finger Pulse Oximeter DP-150 Yellow FDA UDI
Description
The Dagamma DP-150 finger pulse oximeter is a lightweight, portable device used for measuring both heart rate and blood oxygen levels or SpO2. FDA UDI

Identifiers

Primary DI / UDI-DI
00628055787617 FDA UDI
510(k) Number
K082641 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

Yes

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

No

FDA UDI

Category: Pulse oximeter

Dagamma by Dagamma Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dagamma Inc.

Sources (1)

  • FDA UDI dfcdec39-1f08-40c7-a7e5-f0429ad2d170 35 fields · synced Jun 8, 2026