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VivaCart

FDA UDI

Class I (US FDA UDI)

by CardioQuip

Identity

Trade Name
VivaCart FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Model / Reference
Side Mount Single Hook FDA UDI

Identifiers

Catalog Number
VC-D-SH1 FDA UDI
Primary DI / UDI-DI
00850054036087 FDA UDI
FDA Product Code
KRI FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4200 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electromechanical device/system transport trolley

VivaCart by CardioQuip — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CardioQuip

Sources (1)

  • FDA UDI 1844ebe0-c44f-49e6-b383-a99b6b6c9262 34 fields · synced Jun 6, 2026