PHILIPS External Device Interface Module

FDA UDI

Class II (US FDA UDI)

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name: PHILIPS External Device Interface Module FDA UDI
Generic Name: Patient monitoring system module, interfacing FDA UDI
Model / Reference: 862292 FDA UDI

Identifiers

Catalog Number: 862292 FDA UDI
Primary DI / UDI-DI: 00884838021099 FDA UDI
510(k) Number: K923682 FDA UDI
FDA Product Code: MHX FDA UDI
GMDN Term: Patient monitoring system module, interfacing FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1025 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Patient monitoring system module, interfacing

PHILIPS External Device Interface Module by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Philips Medizin Systeme Böblingen GmbH

Sources (1)

FDA UDI 9cc96c98-0155-4686-b3e9-aa9cd829b7cb 35 fields · synced May 30, 2026