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SpO2 Adapter, large, 3/Box

FDA UDIEUDAMED

Class II (US FDA UDI)

by Mipm Mammendorfer Institut Fur Physik Und Medizin

Identity

Trade Name
SpO2 Adapter, large, 3/Box FDA UDI
Generic Name
Pulse Co-oximeter probe, reusable FDA UDI
Model / Reference
SpO2 Adapter, large, 3/Box FDA UDI

Identifiers

Catalog Number
5010013 FDA UDI
Primary DI / UDI-DI
EMIP50100130 FDA UDI
510(k) Number
K142032 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
Pulse Co-oximeter probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Pulse Co-oximeter probe, reusable

SpO2 Adapter, large, 3/Box by Mipm Mammendorfer Institut Fur Physik Und Medizin — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Pulse Co-oximeter probe, reusable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI e5ab247e-b41a-44c7-b042-49528bbadfac 35 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026