Patient Information Center iX 4.7

by Philips Medizin Systeme Böblingen GmbH GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00884838128897 UDI-DI	Date17 Apr 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name: Patient Information Center iX
Generic Name: Centralized patient monitor
Model / Ref / Catalog: 4.7, 866389

Primary DI / UDI-DI: 00884838128897
FDA Product Code: MHX
GMDN Term: Centralized patient monitor

Device Class: Class II
Regulation Number: 870.1025
GUDID distribution status: In Commercial Distribution

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Properties

Prescription Use
Lot / Batch Number

Other properties (12)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No