← Back to catalogue

Maxsplit

EUDAMED

Class I (EU MDR)

Ref BMS02B

by Maxpert Technologies Inc.

Identity

Trade Name
Maxsplit EUDAMED
Device Name
Pill splitter EUDAMED
Model / Reference
BMS02B EUDAMED

Identifiers

Primary DI / UDI-DI
07540161840020 EUDAMED
Basic UDI-DI
754016184PS20BF EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER 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

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

Category: Device sterilization/disinfection container, reusable

Maxsplit by Maxpert Technologies Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CA-MF-000041899
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED ed827664-5152-4bed-b36c-902f9d894f96 61 fields · synced Jun 18, 2026