← Back to catalogue

Care Orchestrator

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Care Orchestrator FDA UDI
Generic Name
Medical equipment clinical data interfacing software FDA UDI
Device Name
Care Orchestrator India FDA UDI
Model / Reference
1.15 FDA UDI
Description
Care Orchestrator India FDA UDI

Identifiers

Catalog Number
1136541 FDA UDI
Primary DI / UDI-DI
00606959052871 FDA UDI
510(k) Number
K152356 FDA UDI
FDA Product Code
MNS FDA UDI
NOU FDA UDI
MNT FDA UDI
BZD FDA UDI
CBK FDA UDI
GMDN Term
Medical equipment clinical data interfacing software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
868.5905 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical equipment clinical data interfacing software

Care Orchestrator by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment clinical data interfacing software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 3c1a007c-1aad-446b-904f-1391ba251b2c 36 fields · synced May 30, 2026