Visia AF MRI™ S VR SureScan™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: Visia AF MRI™ S VR SureScan™ FDA UDI
Generic Name: Single-chamber implantable defibrillator FDA UDI
Device Name: ICD-VR DVFC3D4 VISIA AF MRI S US DF4 FDA UDI
Model / Reference: DVFC3D4 FDA UDI
Description: ICD-VR DVFC3D4 VISIA AF MRI S US DF4 FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000060060 FDA UDI
FDA Product Code: LWS FDA UDI
NVZ FDA UDI
GMDN Term: Single-chamber implantable defibrillator FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Single-chamber implantable defibrillator

Visia AF MRI™ S VR SureScan™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-chamber implantable defibrillator.

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DYNAGEN™ EL ICD VR — Boston Scientific · Class III
Gallant™ — ST. JUDE MEDICAL, INC. · Class III
Paradym RF — MICROPORT CRM SRL · Class III
FORTIFY™ — ST. JUDE MEDICAL, INC. · Class III
Intica 7 VR-T DX DF-1 ProMRI — BIOTRONIK SE & Co. KG · Class III

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 III	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI 5b5fdb4c-185f-42fb-877a-258b8170a86d 35 fields · synced Jun 8, 2026