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Boite Aramis S

EUDAMED

Class I (EU MDR)

Ref ESA BT01Model Class I Instrument

by groupe lépine

Identity

Trade Name
BOITE ARAMIS S EUDAMED
Device Name
Class I Instrument EUDAMED
Model / Reference
Class I Instrument EUDAMED
ESA BT01 EUDAMED

Identifiers

Primary DI / UDI-DI
+M483ESABT010 EUDAMED
Basic UDI-DI
++M483L0999ZW EUDAMED
Direct Marketing DI
+M483ESABT010 EUDAMED
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Boite Aramis S by groupe lépine — 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
groupe lépine
EUDAMED SRN
FR-MF-000001182

Sources (1)

  • EUDAMED 29e83236-bc23-4588-bea3-47f732b8e660 61 fields · synced Jun 17, 2026