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Amadeo

FDA UDIEUDAMED

Class I (US FDA UDI)

by tyromotion GmbH

Identity

Trade Name
AMADEO FDA UDI
Generic Name
Virtual-display rehabilitation system, powered-support, upper-limb FDA UDI
Device Name
The AMADEO system is intended for robot-supported finger-hand therapy of patients with neurological damage to the central nervous system, caused by typical indications such as stroke or traumatic brain injury. FDA UDI
Model / Reference
7 FDA UDI
Description
The AMADEO system is intended for robot-supported finger-hand therapy of patients with neurological damage to the central nervous system, caused by typical indications such as stroke or traumatic brain injury. FDA UDI

Identifiers

Primary DI / UDI-DI
09120077180014 FDA UDI
FDA Product Code
BXB FDA UDI
GMDN Term
Virtual-display rehabilitation system, powered-support, upper-limb FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5380 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Virtual-display rehabilitation system, powered-support, upper-limb

Amadeo by tyromotion GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Virtual-display rehabilitation system, powered-support, upper-limb.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
tyromotion GmbH

Sources (2)

  • FDA UDI fc4d9fa8-f700-4c53-ba89-e26cfba64ff9 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026