Fortify™

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name: FORTIFY™ FDA UDI
Generic Name: Single-chamber implantable defibrillator FDA UDI
Device Name: Tiered-therapy cardioverter/defibrillatorVVEV VVIR FDA UDI
Model / Reference: CD1231-40 FDA UDI
Description: Tiered-therapy cardioverter/defibrillatorVVEV VVIR FDA UDI

Identifiers

Catalog Number: CD1231-40 FDA UDI
Primary DI / UDI-DI: 05414734504355 FDA UDI
FDA Product Code: 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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Total Volume — 35 Milliliter FDA UDI

Category: Single-chamber implantable defibrillator

Fortify™ by St. Jude Medical, Inc. — Class III — 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 III	Pending data

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Manufacturer

Manufacturer: St. Jude Medical, Inc.

Sources (1)

FDA UDI 87e84097-3cff-41b7-b3d2-2d37ca606f1f 37 fields · synced Jun 6, 2026