Care Orchestrator

Care Orchestrator, Clinical data collection management information system application software

Registry build 21.09.26
1manufacturer
10catalogue numbers in this listing
5recalls on this code

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NOU
Manufacturer City Province Registered as Device types
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11

Record

Regulatory record for Care Orchestrator
Listed by Respironics Inc., United States
FDA product code NOU
Device type Continuous, Ventilator, Home Use
Device class Class 2
Regulation 21 CFR 868.5895
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K152356
Record published 2019-06-19
Record revised 2018-11-08 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Care Orchestrator
Catalogue number Size Status
1.22 In distribution
1.14 In distribution
1.16 In distribution
1.9 In distribution
1.3 In distribution
1.10 In distribution
1.15 In distribution
1.21 In distribution
1.15 In distribution
1.12 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vivo 50 Breas Medical, Inc. 17
Patient Circuit Flight Medical Innovations Ltd. 13
Astral Resmed PTY Ltd. 12
Trilogy Evo Respironics Inc. 10
Trilogy Respironics Inc. 10
Trilogy 200 Respironics Inc. 5
Continuous Ventilator Flight Medical Innovations Ltd. 3
Trilogy 100 Respironics Inc. 3
Vocsn Roll Stand Ventec Life Systems, Inc. 2
Sensor Respironics Inc. 2
Astral Double Limb Kit Resmed PTY Ltd. 1
Trilogy EV300 Respironics Inc. 1

Showing 12 of 28. All products under Continuous, Ventilator, Home Use

Recalls

2 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2024-07-16 Class I Device Design Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls. 90,910 US; 56,273 ROW
2024-07-16 Class I Device Design Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls. 90,910 US; 56,273 ROW
2021-07-26 Class II Labeling design Two software issues have been identified related to pressure increase in the device: The first issue is described as “Infant/Pediatric EFS Calibration Pressure Increase” and the second issue is described as “Pressure Drift (Continuous Usage 18936 (US); 4659 (OUS)
2021-07-26 Class II Labeling design Two software issues have been identified related to pressure increase in the device: The first issue is described as “Infant/Pediatric EFS Calibration Pressure Increase” and the second issue is described as “Pressure Drift (Continuous Usage 18588 (US); 5662 (OUS)
2021-07-26 Class II Labeling design Two software issues have been identified related to pressure increase in the device: The first issue is described as “Infant/Pediatric EFS Calibration Pressure Increase” and the second issue is described as “Pressure Drift (Continuous Usage 101 (FEMA Stockpile Only); 21077 (OUS)

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