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LATITUDE® Clarity

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
LATITUDE® Clarity FDA UDI
Generic Name
Patient health record information system application software FDA UDI
Device Name
Device Services Software FDA UDI
Model / Reference
7260 FDA UDI
Description
Device Services Software FDA UDI

Identifiers

Catalog Number
7260 FDA UDI
Primary DI / UDI-DI
00802526613838 FDA UDI
FDA Product Code
MXD FDA UDI
GMDN Term
Patient health record information system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient health record information system application software

LATITUDE® Clarity by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient health record information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 5bdfca1c-110d-4b03-9be2-70fb43fa4a5f 34 fields · synced Jun 6, 2026