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Medistim MiraQ Cardiac System

FDA UDI

Class II (US FDA UDI)

by Medi-Stim Asa

Identity

Trade Name
Medistim MiraQ Cardiac System FDA UDI
Generic Name
Cardiovascular ultrasound imaging system FDA UDI
Model / Reference
MQC14022 FDA UDI

Identifiers

Catalog Number
MQC14022 FDA UDI
Primary DI / UDI-DI
07070554103307 FDA UDI
510(k) Number
K102595 FDA UDI
FDA Product Code
IYO FDA UDI
IYN FDA UDI
DPW FDA UDI
GMDN Term
Cardiovascular ultrasound imaging system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1550 FDA UDI
870.2100 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

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: Cardiovascular ultrasound imaging system

Medistim MiraQ Cardiac System by Medi-Stim Asa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiovascular ultrasound imaging system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medi-Stim Asa

Sources (1)

  • FDA UDI f0f849cd-8026-47e8-8f44-fd5eb7b44c6f 34 fields · synced May 31, 2026