NaviCare® Nurse Call Systems

Hospital Paging System

Registry build 21.09.26
1manufacturer
3catalogue numbers in this listing
1recall

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code ILQ
Manufacturer City Province Registered as Device types
Shenzhen Contin Medical Device Co., Ltd. Shenzhen Guangdong Contract manufacturer 3

Record

Regulatory record for NaviCare® Nurse Call Systems
Listed by Hill-ROM, Inc., United States
FDA product code ILQ
Device type System, Communication, Powered
Device class Class 2
Regulation 21 CFR 890.3710
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2018-12-04
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information

Catalogue Numbers

Catalogue numbers for NaviCare® Nurse Call Systems
Catalogue number Size Status
3.9 In distribution
3.6 In distribution
3.7 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
GEN4 Direct Access Curbell Medical Products, Inc. 1,343
GEN4 Interactive Curbell Medical Products, Inc. 1,005
GEN4 Plus, Direct Access Curbell Medical Products, Inc. 599
Responder 5, Interactive Curbell Medical Products, Inc. 573
Series 8 Anacom MedTek Anacom Medtek 519
Series 7 Anacom MedTek Anacom Medtek 312
GEN4 Plus, Responder 5, Enhanced Curbell Medical Products, Inc. 112
Responder 5, Enhanced Curbell Medical Products, Inc. 108
Tobii Dynavox Tobii Dynavox LLC 44
Nova Chat Prentke Romich Co. 44
GEN4 Plus, Responder 5, Standard Curbell Medical Products, Inc. 33
Saltillo Prentke Romich Co. 27

Showing 12 of 1,439. All products under System, Communication, Powered

Recalls Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of NaviCare® Nurse Call Systems
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Baxter Healthcare Corporation UDI-DI 2022-04-13 Class II Software design Firm discovered a firmware memory leak with a supplier-manufactured component. 11028 units 2023-12-20
Hill-ROM, Inc. UDI-DI 2021-10-14 Class II Under Investigation by firm An unrecoverable error may occur where a component will fail to complete the reboot cycle, become non-functional and must be replaced. 1,050 units 2024-08-16

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer