Mural Clinical Viewer

FDA UDI

Class II (US FDA UDI)

by Ge Medical Systems Information Technologies, Inc.

Identity

Trade Name: Mural Clinical Viewer FDA UDI
Generic Name: Patient health record information system FDA UDI
Device Name: MD Mural Clinical Viewer 1.2 MEDICAL DEVICE FDA UDI
Model / Reference: 1.2 FDA UDI
Description: MD Mural Clinical Viewer 1.2 MEDICAL DEVICE FDA UDI

Identifiers

Primary DI / UDI-DI: 00195278789846 FDA UDI
510(k) Number: K222586 FDA UDI
FDA Product Code: MHX FDA UDI
GMDN Term: Patient health record information system 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

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Patient health record information system

Mural Clinical Viewer by Ge Medical Systems Information Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Home Monitoring Service Center — BIOTRONIK SE & Co. KG · Class III
ELI Edit — MORTARA INSTRUMENT, INC. · Class II
ESSENZ — LivaNova Deutschland GmbH · Class II
Datapad — LivaNova Deutschland GmbH · Class II

Cleared under the same submission

K222586 also covers:

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: Ge Medical Systems Information Technologies, Inc.

Sources (1)

FDA UDI 6de70a8e-54e8-473a-925e-c8c3258abd57 34 fields · synced Jun 8, 2026