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Ultrasonic Surgical Instrument

EUDAMED

Class IIb (EU MDR)

Ref POA-23 Pro7iModel POA-14 Pro

by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Identity

Device Name
Ultrasonic Surgical Instrument EUDAMED
Model / Reference
POA-14 Pro EUDAMED
POA-23 Pro7i EUDAMED

Identifiers

Primary DI / UDI-DI
06903053134231 EUDAMED
Basic UDI-DI
69449040AB0511000462 EUDAMED
EMDN Code
K0202010201,K0202010202 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Ultrasonic Surgical Instrument by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000014156
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED daf9543c-55a3-4d2f-8b25-4cdf2734fa46 61 fields · synced Jun 18, 2026