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Vendor Neutral Archive with ConnectWeb

FDA UDI

Class I (US FDA UDI)

by Radius Corporation

Identity

Trade Name
Vendor Neutral Archive with ConnectWeb FDA UDI
Generic Name
Radiological PACS software FDA UDI
Device Name
PACSCore VNA archive with remote, remote backup, and optional local repositories, and ConnectWeb on remote archive FDA UDI
Model / Reference
7 FDA UDI
Description
PACSCore VNA archive with remote, remote backup, and optional local repositories, and ConnectWeb on remote archive FDA UDI

Identifiers

Primary DI / UDI-DI
B295VNA70 FDA UDI
FDA Product Code
LMD FDA UDI
GMDN Term
Radiological PACS software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2020 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

No

FDA UDI

Category: Radiological PACS software

Vendor Neutral Archive with ConnectWeb by Radius Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological PACS software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Radius Corporation

Sources (1)

  • FDA UDI e92dbf29-bfea-4fc4-9eeb-f6ec2eea13b5 33 fields · synced May 30, 2026