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Retractors/Earabeup

EUDAMED

Class I (EU MDR)

Ref Retractors/Earabeup

by Qureshi Manufacturing Corporation

Identity

Device Name
Retractors/Earabeup EUDAMED
Model / Reference
Retractors/Earabeup EUDAMED

Identifiers

Primary DI / UDI-DI
111823013720 EUDAMED
Basic UDI-DI
PP12633RETRACTORSEAR18 EUDAMED
Direct Marketing DI
111823013720 EUDAMED
EMDN Code
L03140101 SELF-STATIC SPREADERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria 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

Retractors/Earabeup by Qureshi Manufacturing Corporation — 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

EUDAMED SRN
PK-MF-000024744
Authorised Representative
AF Pharma Service Europe SL ES-AR-000018076

Sources (1)

  • EUDAMED fdc7e8b9-00ff-498b-937e-21533c7af52c 61 fields · synced Jun 18, 2026