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Dolphin

FDA UDI

Class II (US FDA UDI)

by Osi Optoelectronics, Inc.

Identity

Trade Name
Dolphin FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
Adult Disposable Oximetry Sensor FDA UDI
Model / Reference
3311-F FDA UDI
Description
Adult Disposable Oximetry Sensor FDA UDI

Identifiers

Primary DI / UDI-DI
00859998006255 FDA UDI
510(k) Number
K030952 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulse oximeter probe, single-use

Dolphin by Osi Optoelectronics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, single-use.

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 b0c7cfd6-0b77-4a85-97b0-6a9d19dd3b45 34 fields · synced May 29, 2026