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Pergo

EUDAMED

Class I (EU MDR)

Ref 05TD0010

by Pergo Medikal ve Ilac Sanayi A.S.

Identity

Trade Name
Pergo EUDAMED
Device Name
Biopsy Valve (Olympus-Fujinon Sterile) EUDAMED
Model / Reference
05TD0010 EUDAMED

Identifiers

Primary DI / UDI-DI
08681756010615 EUDAMED
Basic UDI-DI
B-08681756010615 EUDAMED
EMDN Code
G0380 DIGESTIVE ENDOSCOPY DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Gastro-urological guidewire, single-use

Pergo by Pergo Medikal ve Ilac Sanayi A.S. — Class I — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological guidewire, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000020761

Sources (1)

  • EUDAMED b937983f-dc58-4a1c-a484-3eb5314cee74 61 fields · synced Oct 8, 2026