← Back to catalogue

Regulated Software Application (RSA)

FDA UDI

Class II (US FDA UDI)

by Arc-One Solutions, Llc

Identity

Trade Name
Regulated Software Application (RSA) FDA UDI
Generic Name
Blood bank information system application software FDA UDI
Device Name
The Regulated Software Application (RSA) is a system of co-dependent web based computer programs, used to manage and support all aspects of the blood banking process. FDA UDI
Model / Reference
1.0.33.0 FDA UDI
Description
The Regulated Software Application (RSA) is a system of co-dependent web based computer programs, used to manage and support all aspects of the blood banking process. FDA UDI

Identifiers

Catalog Number
1.0.33.0 FDA UDI
Primary DI / UDI-DI
00860003545409 FDA UDI
FDA Product Code
MMH FDA UDI
GMDN Term
Blood bank information system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9165 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Regulated Software Application (RSA) by Arc-One Solutions, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 65e232db-0c6c-4f25-be06-bd612f8a8f02 37 fields · synced May 30, 2026