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ACPlus Platform

FDA UDI

Class I (US FDA UDI)

by Accelerated Care Plus Corp.

Identity

Trade Name
ACPlus Platform FDA UDI
Generic Name
Medical equipment clinical data interfacing software FDA UDI
Device Name
Medical equipment clinical data interfacing software FDA UDI
Model / Reference
100ACPLUS FDA UDI
Description
Medical equipment clinical data interfacing software FDA UDI

Identifiers

Primary DI / UDI-DI
00858703006368 FDA UDI
FDA Product Code
ION FDA UDI
GMDN Term
Medical equipment clinical data interfacing software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5370 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

Category: Medical equipment clinical data interfacing software

ACPlus Platform by Accelerated Care Plus Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment clinical data interfacing software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accelerated Care Plus Corp.

Sources (1)

  • FDA UDI 9d57b520-8ede-4afe-b293-3d346b4acae0 34 fields · synced May 30, 2026