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ComboMap Pressure and Flow System

FDA UDI

Class II (US FDA UDI)

by Volcano Corporation

Identity

Trade Name
ComboMap Pressure and Flow System FDA UDI
Generic Name
Intravascular haemodynamic monitoring system FDA UDI
Model / Reference
6800 FDA UDI

Identifiers

Catalog Number
802745001 FDA UDI
Primary DI / UDI-DI
00845225010874 FDA UDI
FDA Product Code
OBJ FDA UDI
IYO FDA UDI
GMDN Term
Intravascular haemodynamic monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 FDA UDI
892.1560 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: Intravascular haemodynamic monitoring system

ComboMap Pressure and Flow System by Volcano Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular haemodynamic monitoring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Volcano Corporation

Sources (1)

  • FDA UDI 44758c28-79b3-49d4-9e2b-63583f3d5c66 33 fields · synced Jun 8, 2026