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Archimedes® System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 40005

by Broncus Medical, Inc.

Identity

Trade Name
Archimedes® System EUDAMED
Archimedes System FDA UDI
Generic Name
Virtual bronchoscopic navigation PACS software FDA UDI
Device Name
Archimedes System EUDAMED
Archimedes software is installed on a desktop computer used to plan procedures and navigate to targets in the lung. The Procedure Module offers real-time navigation guidance for use during the bronchoscopy procedure. The Software provides the option to segment previously acquired CT or other DICOM data sets and overlay and register these segmented data sets onto live fluoroscopic X-ray images. The software allows visualization of the bronchial tree; helps guide the tools in or adjacent to the bronchial tree; allows visualization of a predefined target in lung tissue; and assists with placement of markers into soft lung tissue to guide radiosurgery and thoracic surgery. FDA UDI
Model / Reference
40005 EUDAMEDFDA UDI
Description
Archimedes software is installed on a desktop computer used to plan procedures and navigate to targets in the lung. The Procedure Module offers real-time navigation guidance for use during the bronchoscopy procedure. The Software provides the option to segment previously acquired CT or other DICOM data sets and overlay and register these segmented data sets onto live fluoroscopic X-ray images. The software allows visualization of the bronchial tree; helps guide the tools in or adjacent to the bronchial tree; allows visualization of a predefined target in lung tissue; and assists with placement of markers into soft lung tissue to guide radiosurgery and thoracic surgery. FDA UDI

Identifiers

Catalog Number
40005 FDA UDI
Primary DI / UDI-DI
00856571007036 EUDAMEDFDA UDI
Basic UDI-DI
B-00856571007036 EUDAMED
510(k) Number
K133385 FDA UDI
FDA Product Code
LLZ FDA UDI
EMDN Code
R0799 BRONCOPULMONARY ENDOSCOPY DEVICES, SINGLE-USE - OTHER EUDAMED
GMDN Term
Virtual bronchoscopic navigation PACS software FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.2050 FDA UDI
Special Device Type
-1192 EUDAMED
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Archimedes® System by Broncus Medical Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000027543
Authorised Representative
MedDevConsult GmbH DE-AR-000005877

Sources (2)

  • EUDAMED 2da20eea-0624-4a2f-b7cf-e4be8ae3b94e 61 fields · synced Jul 17, 2026
  • FDA UDI 467aa96c-d80f-424a-8336-f55bb0c3609f 37 fields · synced May 30, 2026