← Back to catalogue

IMPAX Clinical Applications

FDA UDI

Class II (US FDA UDI)

by Agfa Healthcare Corp.

Identity

Trade Name
IMPAX Clinical Applications FDA UDI
Generic Name
Radiological PACS software FDA UDI
Device Name
IMPAX Volume Viewing and IMPAX PET & SPECT Viewing FDA UDI
Model / Reference
4 FDA UDI
Description
IMPAX Volume Viewing and IMPAX PET & SPECT Viewing FDA UDI

Identifiers

Primary DI / UDI-DI
05400874001205 FDA UDI
510(k) Number
K080013 FDA UDI
K111638 FDA UDI
K133135 FDA UDI
K161061 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiological PACS software

IMPAX Clinical Applications by Agfa Healthcare Corp. — Class II — 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

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

Manufacturer

Sources (1)

  • FDA UDI 689c17b6-8e2c-44b3-9cdf-3a77c24eb36c 35 fields · synced May 30, 2026