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Pediatric Flow Probe 1/4" X 3/32"

FDA UDI

Class II (US FDA UDI)

by Thoratec Switzerland GmbH

Identity

Trade Name
PEDIATRIC FLOW PROBE 1/4" X 3/32" FDA UDI
Generic Name
Extracorporeal fluid flow probe FDA UDI
Model / Reference
104298 FDA UDI

Identifiers

Catalog Number
104298 FDA UDI
Primary DI / UDI-DI
07640135140146 FDA UDI
FDA Product Code
KFM FDA UDI
GMDN Term
Extracorporeal fluid flow probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4360 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

Category: Extracorporeal fluid flow probe

Pediatric Flow Probe 1/4" X 3/32" by Thoratec Switzerland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI eb04f4ca-cacd-48af-a025-8a7a36cdb77e 35 fields · synced Jun 8, 2026