← Back to catalogue

CENTRIMAG™ System Transporter

FDA UDI

Class I (US FDA UDI)

by Thoratec Switzerland GmbH

Identity

Trade Name
CENTRIMAG™ System Transporter FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
System Transporter FDA UDI
Model / Reference
201-50140 FDA UDI
Description
System Transporter FDA UDI

Identifiers

Catalog Number
201-50140 FDA UDI
Primary DI / UDI-DI
07640135140771 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electromechanical device/system transport trolley

CENTRIMAG™ System Transporter by Thoratec Switzerland GmbH — 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

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

Manufacturer

Manufacturer
Thoratec Switzerland GmbH

Sources (1)

  • FDA UDI c48bf466-2d28-4884-b9a9-72f3b2bd4c4c 36 fields · synced Jun 8, 2026