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Aortic Aneurysm Large

EUDAMED

Class IIa (EU MDR)

Ref SO46124CModel Thompson Retractor System

by Thompson Surgical Instruments, Inc.

Identity

Trade Name
Aortic Aneurysm Large EUDAMED
Model / Reference
Thompson Retractor System EUDAMED
SO46124C EUDAMED

Identifiers

Primary DI / UDI-DI
00841536125795 EUDAMED
Basic UDI-DI
008415361TRMR EUDAMED
Direct Marketing DI
00841536125795 EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Surgical retraction system, reusable

Aortic Aneurysm Large by Thompson Surgical Instruments, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000013232
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED ef1fc68a-9227-4a40-8640-0ddfdf78d55a 61 fields · synced Jul 17, 2026