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Butler Palpeter

EUDAMED

Class I (EU MDR)

Ref 99P8000

by Sunstar Europe SA

Identity

Trade Name
BUTLER PALPETER EUDAMED
Device Name
BUTLER PALPETER EUDAMED
Model / Reference
99P8000 EUDAMED

Identifiers

Primary DI / UDI-DI
17630019900192 EUDAMED
Basic UDI-DI
B-17630019900192 EUDAMED
EMDN Code
Z12040101 ALGESIMETERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Butler Palpeter by Sunstar Europe SA — Class I — 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

Manufacturer
Sunstar Europe SA
EUDAMED SRN
CH-MF-000023162
Authorised Representative
Sunstar France FR-AR-000018318

Sources (1)

  • EUDAMED 579a8268-f8d6-406e-b2dd-288d463917f8 61 fields · synced Oct 6, 2026