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ScoutPro Osmolarity System

FDA UDI

Class I (US FDA UDI)

by Tearlab Corporation

Identity

Trade Name
ScoutPro Osmolarity System FDA UDI
Generic Name
Osmometric analyser IVD FDA UDI
Device Name
In-vitro analysis of ocular tear fluid. FDA UDI
Model / Reference
100094 FDA UDI
Description
In-vitro analysis of ocular tear fluid. FDA UDI

Identifiers

Primary DI / UDI-DI
00853539002188 FDA UDI
FDA Product Code
OND FDA UDI
GMDN Term
Osmometric analyser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1540 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Osmometric analyser IVD

ScoutPro Osmolarity System by Tearlab Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Osmometric analyser IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tearlab Corporation

Sources (1)

  • FDA UDI 4009cb79-d026-46cd-a6f9-9de742172f92 33 fields · synced May 30, 2026