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PatientCare Link

FDA UDI

Class II (US FDA UDI)

by Preventice Technologies, Inc.

Identity

Trade Name
PatientCare Link FDA UDI
Generic Name
Cardiopulmonary physiological parameter analysis software FDA UDI
Device Name
Upload and transmission software application FDA UDI
Model / Reference
SW1004 FDA UDI
Description
Upload and transmission software application FDA UDI

Identifiers

Primary DI / UDI-DI
00852132007316 FDA UDI
FDA Product Code
DSI FDA UDI
GMDN Term
Cardiopulmonary physiological parameter analysis 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cardiopulmonary physiological parameter analysis software

PatientCare Link by Preventice Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary physiological parameter analysis software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Preventice Technologies, Inc.

Sources (1)

  • FDA UDI 04e10ae4-4f40-49d3-b18d-fe8b173f471b 33 fields · synced May 30, 2026