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MeMed Key®

EUDAMEDFDA UDI

Class A (EU MDR)

Ref FG130001

by MeMed Diagnostics Ltd.

Identity

Trade Name
MeMed Key® EUDAMEDFDA UDI
Generic Name
Chemiluminescent immunoassay analyser IVD FDA UDI
Device Name
MeMed Key® EUDAMED
Model / Reference
FG130001 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
17290018739003 EUDAMEDFDA UDI
Basic UDI-DI
729001873900CS EUDAMED
Direct Marketing DI
17290018739003 EUDAMED
510(k) Number
K210254 FDA UDI
FDA Product Code
QPS FDA UDI
EMDN Code
W0299 IVD INSTRUMENTS - OTHER EUDAMED
GMDN Term
Chemiluminescent immunoassay analyser IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
866.3215 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

MeMed Key® by Memed Diagnostics Ltd — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
IL-MF-000023622
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED f8df802a-84cf-4cac-a3d0-69f14d870946 61 fields · synced Jun 18, 2026
  • FDA UDI 88cf4e11-830c-4176-a5f6-3a0caeff1f41 33 fields · synced May 29, 2026