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X-Ray FootStep

EUDAMED

Class I (EU MDR)

Ref 1277-AModel X-Ray FootStep

by Pearl Technology AG

Identity

Trade Name
X-Ray FootStep EUDAMED
Device Name
X-Ray FootStep EUDAMED
Model / Reference
X-Ray FootStep EUDAMED
1277-A EUDAMED

Identifiers

Primary DI / UDI-DI
07640178061798 EUDAMED
Basic UDI-DI
764017806FootStepQ9 EUDAMED
Direct Marketing DI
07640178061798 EUDAMED
EMDN Code
Z11079080 VARIOUS SUPPORTING INSTRUMENTS FOR X-RAY FILM SYSTEM - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Malta EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

X-Ray FootStep by Pearl Technology Ag — 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

Manufacturer
Pearl Technology AG
EUDAMED SRN
CH-MF-000018100
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 42336331-a2cc-4ca1-b053-192661e1df6e 61 fields · synced Jul 14, 2026