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Viva™ XT CRT-D

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Viva™ XT CRT-D FDA UDI
Generic Name
Cardiac resynchronization therapy implantable defibrillator FDA UDI
Device Name
CRTD DTBA1D1 VIVA XT US IS1/DF1 FDA UDI
Model / Reference
DTBA1D1 FDA UDI
Description
CRTD DTBA1D1 VIVA XT US IS1/DF1 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000059545 FDA UDI
FDA Product Code
KRG FDA UDI
NIK FDA UDI
GMDN Term
Cardiac resynchronization therapy implantable defibrillator FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.3700 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

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

No

FDA UDI

Category: Cardiac resynchronization therapy implantable defibrillator

Viva™ XT CRT-D by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac resynchronization therapy implantable defibrillator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 3c9ad0d2-8345-4d83-b8d5-b0e1fd6f4e5a 35 fields · synced May 30, 2026