Avvigo™+

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name: AVVIGO™+ FDA UDI
Generic Name: Cardiovascular ultrasound imaging system FDA UDI
Device Name: Multi-Modality Guidance System FDA UDI
Model / Reference: H7492493022R0 FDA UDI
Description: Multi-Modality Guidance System FDA UDI

Identifiers

Catalog Number: H7492493022R0 FDA UDI
Primary DI / UDI-DI: 00191506033019 FDA UDI
FDA Product Code: DQK FDA UDI
ITX FDA UDI
IYO FDA UDI
DSK FDA UDI
GMDN Term: Cardiovascular ultrasound imaging system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1425 FDA UDI
892.1570 FDA UDI
892.1560 FDA UDI
870.1110 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiovascular ultrasound imaging system

Avvigo™+ by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Boston Scientific

Sources (1)

FDA UDI 895627f1-a66d-4894-92ab-fec32d6260d1 34 fields · synced Jun 6, 2026