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VitalStream

FDA UDI

Class II (US FDA UDI)

by Caretaker Medical, LLC

Identity

Trade Name
VitalStream FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Wireless Vital Signs Monitor FDA UDI
Model / Reference
CT5 FDA UDI
Description
Wireless Vital Signs Monitor FDA UDI

Identifiers

Catalog Number
CT-VS-SM, CT-VS-CM, CT-VS-HM FDA UDI
Primary DI / UDI-DI
00864609000317 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: General-purpose multi-parameter bedside monitor

VitalStream by Caretaker Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caretaker Medical, LLC

Sources (1)

  • FDA UDI 1916b7dc-ee03-4f23-947e-20ded8005083 36 fields · synced May 30, 2026