← Back to catalogue

Media Writer

FDA UDI

Class I (US FDA UDI)

by Hyland Llc

Identity

Trade Name
Media Writer FDA UDI
Generic Name
Radiology DICOM image processing application software FDA UDI
Device Name
Media Writer Software FDA UDI
Model / Reference
5 FDA UDI
Description
Media Writer Software FDA UDI

Identifiers

Primary DI / UDI-DI
00850677007129 FDA UDI
FDA Product Code
LMD FDA UDI
GMDN Term
Radiology DICOM image processing application 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiology DICOM image processing application software

Media Writer by Hyland Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiology DICOM image processing application 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

Manufacturer
Hyland Llc

Sources (1)

  • FDA UDI ec8d5acb-6883-4afd-bb79-dcb5e5c06911 34 fields · synced May 31, 2026