← Back to catalogue

Starling SV

FDA UDI

Class II (US FDA UDI)

by Cheetah Medical (israel) Ltd

Identity

Trade Name
Starling SV FDA UDI
Generic Name
Multiple vital physiological parameter monitoring system, clinical FDA UDI
Device Name
A portable, non-invasive cardiac output (CO) monitoring device. FDA UDI
Model / Reference
CMM-ST5 FDA UDI
Description
A portable, non-invasive cardiac output (CO) monitoring device. FDA UDI

Identifiers

Catalog Number
CMM-ST5 FDA UDI
Primary DI / UDI-DI
07290013030030 FDA UDI
FDA Product Code
DSB FDA UDI
DXN FDA UDI
GMDN Term
Multiple vital physiological parameter monitoring system, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 FDA UDI
870.1130 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Starling SV by Cheetah Medical (israel) Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI c4430769-87c1-4b76-8944-caf45476dff3 37 fields · synced May 30, 2026