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TraumaCad

FDA UDI

Class II (US FDA UDI)

by Brainlab AG

Identity

Trade Name
TraumaCad FDA UDI
Generic Name
Radiological PACS software FDA UDI
Model / Reference
2.5 FDA UDI

Identifiers

Primary DI / UDI-DI
07290109941004 FDA UDI
510(k) Number
K073714 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

TraumaCad by Brainlab AG — 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

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Manufacturer

Manufacturer
Brainlab AG

Sources (1)

  • FDA UDI d874cd82-fa50-40d9-8006-50eded4fc0ef 34 fields · synced Jun 1, 2026