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iBEAM evo Couch Adapter

EUDAMEDFDA UDI

Class I (EU MDR)

Ref P10105-149

by 3C-Medical Intelligence GmbH

Identity

Trade Name
iBEAM evo Couch Adapter EUDAMED
iBEAM FDA UDI
Generic Name
Accelerator system table, non-powered FDA UDI
Device Name
iBEAM evo Couchtop, iBEAM one Couchtop EUDAMED
iBEAM® evo Couch Adapter allows mounting of the BrainLAB Couchmount System for Varian Exact. FDA UDI
Model / Reference
P10105-149 EUDAMEDFDA UDI
Description
iBEAM® evo Couch Adapter allows mounting of the BrainLAB Couchmount System for Varian Exact. FDA UDI

Identifiers

Catalog Number
P10105-149 FDA UDI
Primary DI / UDI-DI
04056719001063 EUDAMEDFDA UDI
Basic UDI-DI
04056719BUDI0000000003HY EUDAMED
Direct Marketing DI
04056719001063 EUDAMED
FDA Product Code
IXQ FDA UDI
EMDN Code
Z11019080 VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Accelerator system table, non-powered FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
Market of Registration
Germany 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multi-modality therapeutic radiation phantom, test object

iBEAM evo Couch Adapter by 3C-Medical Intelligence GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality therapeutic radiation phantom, test object.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
DE-MF-000023763

Sources (2)

  • EUDAMED ab093e42-e7f5-42e0-bc2e-96b2ee78e197 61 fields · synced Jun 19, 2026
  • FDA UDI 0c62c63a-f363-42c6-930f-ea3f127a133a 34 fields · synced May 30, 2026