LATITUDE Consult™

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name: LATITUDE Consult™ FDA UDI
Generic Name: Cardiac pulse generator software FDA UDI
Device Name: LATITUDE Consult™ System FDA UDI
Model / Reference: 6294 FDA UDI
Description: LATITUDE Consult™ System FDA UDI

Identifiers

Primary DI / UDI-DI: 00802526562907 FDA UDI
PMA Number: P910077 FDA UDI
FDA Product Code: OSR FDA UDI
GMDN Term: Cardiac pulse generator software FDA UDI

Classification

Device Class: Class III 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Cardiac pulse generator software

LATITUDE Consult™ by Boston Scientific — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac pulse generator software.

ON-Q* Pain Relief System — Avanos Medical, Inc. · Class II
LATITUDE Consult™ — Boston Scientific · Class III

Cleared under the same submission

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Boston Scientific

Sources (1)

FDA UDI e3a7fb4a-4623-4764-b688-21683a834235 34 fields · synced May 31, 2026