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Pathfinder SL

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Pathfinder SL FDA UDI
Generic Name
Cardiology information system application software FDA UDI
Device Name
SENTINEL 11 / PATHFINDER SL KIT ES FDA UDI
Model / Reference
98000; 98200 FDA UDI
Description
SENTINEL 11 / PATHFINDER SL KIT ES FDA UDI

Identifiers

Catalog Number
040-1750-01 FDA UDI
Primary DI / UDI-DI
10841522125843 FDA UDI
FDA Product Code
DQK FDA UDI
GMDN Term
Cardiology information system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1425 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

Yes

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: Electrocardiographic long-term ambulatory recording analyserCardiology information system application software

Pathfinder SL by Spacelabs Healthcare (washington), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiology information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f72c47d-79be-404c-80d2-e54d20788cc9 34 fields · synced Jun 1, 2026