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PatientCare

FDA UDI

Class I (US FDA UDI)

by Wallac, Inc.

Identity

Trade Name
PatientCare FDA UDI
Generic Name
Clinical laboratory information system FDA UDI
Device Name
Specimen Gate® PatientCare™ is intended for management of the follow-up workflow of a screening system. FDA UDI
Model / Reference
5002-0130 FDA UDI
Description
Specimen Gate® PatientCare™ is intended for management of the follow-up workflow of a screening system. FDA UDI

Identifiers

Catalog Number
5002-0130 FDA UDI
Primary DI / UDI-DI
06438147153275 FDA UDI
FDA Product Code
JQP FDA UDI
GMDN Term
Clinical laboratory information system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2100 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Clinical laboratory information system

PatientCare by Wallac, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical laboratory information system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wallac, Inc.

Sources (1)

  • FDA UDI cf49630b-aeae-48d4-b65b-849d707e01f0 34 fields · synced Jun 1, 2026