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Organization name
UDI-DI code
Reference / catalog number

Wi-3 Probe — Class IIa MDR by A.M.I. Agency for…

MD Atlas
A.M.I. Agency for Medical Innovations GmbH

EUDAMED last updated this device on Aug 29, 2025

Wi-3 Probe

++EAMIA45B4C1D2MP

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: A.M.I. Agency for Medical Innovations GmbH
UDI-DI code: +EAMITRI20111
Reference / catalog number: TRI2011

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Manufacturer information

Organization name: A.M.I. Agency for Medical Innovations GmbH
SRN: AT-MF-000016792
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Germany		Still on market

Device identification

Trade name: Wi-3 Probe
UDI-DI code: +EAMITRI20111
Basic UDI-DI: ++EAMIA45B4C1D2MP
Reference / catalog number: TRI2011
Issuing entity: HIBCC

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 5
Additional product description: —
Additional information URL: https://www.ami.at/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G020401HAEMORRHOID LIGATURE SETS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification