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V-Grad 40

EUDAMEDFDA 510(k)

Class III (EU MDR)

Ref V-GRD43_100G

by VITROMED GmbH

Identity

Trade Name
V-GRAD 40 EUDAMED
Device Name
V-GRAD 40 EUDAMED
Model / Reference
V-GRD43_100G EUDAMED

Identifiers

Primary DI / UDI-DI
04260531791587 EUDAMED
Basic UDI-DI
B-04260531791587 EUDAMED
EMDN Code
U08020502 MATERIALS/SOLUTIONS FOR PREPARATION/HANDLING FOR ASSISTED REPRODUCTION EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

V-Grad 40 by VITROMED GmbH — Class III — FDA_510K, MDD — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDD

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Manufacturer

Manufacturer
VITROMED GmbH
EUDAMED SRN
DE-MF-000005131

Sources (2)

  • EUDAMED d442eb1a-027a-4fb8-8ae3-d8ad98c500ee 61 fields · synced Jun 19, 2026
  • FDA 510(k) K241833 1 fields · synced May 18, 2026