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Supra Explorer

EUDAMED

Class III (EU MDR)

Ref FGTX225016

by Sahajanand Medical Technologies Limited

Identity

Trade Name
Supra Explorer EUDAMED
Device Name
Supra Explorer EUDAMED
Model / Reference
FGTX225016 EUDAMED

Identifiers

Primary DI / UDI-DI
08904442303144 EUDAMED
Basic UDI-DI
B-08904442303144 EUDAMED
EMDN Code
P070402010301 CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

Supra Explorer by Sahajanand Medical Technologies Limited — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IN-MF-000016582
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 92e9a1b0-5675-4b8b-957a-6c5ba3571d12 61 fields · synced Jul 8, 2026