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Nonin

FDA UDI

Class II (US FDA UDI)

by Nonin Medical, Inc.

Identity

Trade Name
Nonin FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
Xpod LP with 7000A, 6000CA for use with GE ApexPro CH FDA UDI
Model / Reference
3013 CH FDA UDI
Description
Xpod LP with 7000A, 6000CA for use with GE ApexPro CH FDA UDI

Identifiers

Primary DI / UDI-DI
00833166001242 FDA UDI
510(k) Number
K093853 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Pulse oximeter probe, single-usePulse oximeterPulse oximeter, line-powered

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

Similar devices

Also classified as Pulse oximeter, line-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nonin Medical, Inc.

Sources (1)

  • FDA UDI 3e895456-0ec9-4a98-8428-0cb1818e93e7 37 fields · synced Jun 9, 2026