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Em-Tec Pediatric Flow Probe For 2nd Gen Centrimag Primary Console

FDA UDI

Class II (US FDA UDI)

by Thoratec Switzerland GmbH

Identity

Trade Name
EM-TEC PEDIATRIC FLOW PROBE FOR 2ND GEN CENTRIMAG PRIMARY CONSOLE FDA UDI
Generic Name
Extracorporeal fluid flow probe FDA UDI
Model / Reference
201-30107 FDA UDI

Identifiers

Catalog Number
201-30107 FDA UDI
Primary DI / UDI-DI
07640135140115 FDA UDI
FDA Product Code
DWA FDA UDI
GMDN Term
Extracorporeal fluid flow probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4380 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

Yes

FDA UDI

Category: Extracorporeal fluid flow probe

Em-Tec Pediatric Flow Probe For 2nd Gen Centrimag Primary Console by Thoratec Switzerland GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Extracorporeal fluid flow probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thoratec Switzerland GmbH

Sources (1)

  • FDA UDI 618e5f31-e492-4d11-81b6-dc2997283a5f 35 fields · synced Jun 8, 2026