← Back to catalogue

Blackford Platform

FDA UDI

Class II (US FDA UDI)

by Blackford Analysis, Ltd.

Identity

Trade Name
Blackford Platform FDA UDI
Generic Name
Radiological PACS software FDA UDI
Device Name
Blackford Platform v2.3.x, supplied with Blackford Smart Localizer (part of the Blackford Product Family) FDA UDI
Model / Reference
2.3.x FDA UDI
Description
Blackford Platform v2.3.x, supplied with Blackford Smart Localizer (part of the Blackford Product Family) FDA UDI

Identifiers

Primary DI / UDI-DI
05060570830099 FDA UDI
510(k) Number
K142337 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Radiological PACS software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiological PACS software

Blackford Platform by Blackford Analysis, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological PACS software.

Cleared under the same submission

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 22639f90-8e23-48c2-8add-b4b89e658319 35 fields · synced May 30, 2026