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DICOM Proxy

FDA UDI

Class I (US FDA UDI)

by Brainlab SE

Identity

Trade Name
DICOM Proxy FDA UDI
Generic Name
Radiology picture archiving and communication system workstation FDA UDI
Model / Reference
4.1 FDA UDI

Identifiers

Primary DI / UDI-DI
04056481140519 FDA UDI
FDA Product Code
LMD FDA UDI
GMDN Term
Radiology picture archiving and communication system workstation FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2020 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

DICOM Proxy by Brainlab SE — Class I — 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

Manufacturer
Brainlab SE

Sources (1)

  • FDA UDI a006ba7d-e12b-4278-a6d9-1ed02b703f6d 33 fields · synced May 30, 2026