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Enlarger™Pro

EUDAMED

Class I (EU MDR)

Ref 2052050Model 191020SRef 2052050S

by APT Medical Inc.

Identity

Trade Name
Enlarger™Pro EUDAMED
Device Name
Enlarger™ Inflation Device EUDAMED
Model / Reference
191020S EUDAMED
2052050 EUDAMED
2052050S EUDAMED

Identifiers

Primary DI / UDI-DI
06931896162005 EUDAMED
06931896161992 EUDAMED
Basic UDI-DI
69494504IFD19R6 EUDAMED
EMDN Code
C01040180 CORONARY ANGIOGRAPHY DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Enlarger™Pro by APT Medical Inc. — Class I — 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

Manufacturer
APT Medical Inc.
EUDAMED SRN
CN-MF-000009046
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED 9fa203f9-4298-4cb5-9153-d5cd0be42dfb 61 fields · synced Jul 20, 2026
  • EUDAMED e7ee8aab-c2e5-46be-b160-ee3ce58b1b20 61 fields · synced May 17, 2026