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Centrimag Rvas Hde Kit

FDA UDI

Class Unclassified (US FDA UDI)

by Thoratec Switzerland GmbH

Identity

Trade Name
CENTRIMAG RVAS HDE KIT FDA UDI
Generic Name
External ventricular circulatory assist system FDA UDI
Model / Reference
104318 FDA UDI

Identifiers

Catalog Number
104318 FDA UDI
Primary DI / UDI-DI
07640135140603 FDA UDI
FDA Product Code
OJE FDA UDI
GMDN Term
External ventricular circulatory assist system FDA UDI

Classification

Device Class
Unclassified FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External ventricular circulatory assist system

Centrimag Rvas Hde Kit by Thoratec Switzerland GmbH — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External ventricular circulatory assist system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a2cf1e96-1b00-42a2-8b16-8eb162b4d7dc 35 fields · synced Jun 8, 2026