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Pump with Topical Actuator

EUDAMED

Class I (EU MDR)

Ref SC-JModel CR-3";CR-CM;CR-DP1;CR-I;CR-J;CR-L;CR-LF;CR-LR;CR-MM;CR-N;CR-NM;CR-NM1;CR-O;CR-OL;CR-SF1;CR-SF2;CR-SF3;CR-SR;SC-3";SC-DP1;SC-J;SC-L;SC-LF;etc

by Shenzhen Bona Pharma Technology Co., Ltd.

Identity

Device Name
Pump with Topical Actuator EUDAMED
Model / Reference
CR-3";CR-CM;CR-DP1;CR-I;CR-J;CR-L;CR-LF;CR-LR;CR-MM;CR-N;CR-NM;CR-NM1;CR-O;CR-OL;CR-SF1;CR-SF2;CR-SF3;CR-SR;SC-3";SC-DP1;SC-J;SC-L;SC-LF;etc EUDAMED
SC-J EUDAMED

Identifiers

Primary DI / UDI-DI
06976262371285 EUDAMED
Basic UDI-DI
697626237BNPTAP8 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Pump with Topical Actuator by Shenzhen Bona Pharma Technology Co., Ltd. — 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

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Manufacturer

EUDAMED SRN
CN-MF-000017363
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 88e52b07-8eeb-47bc-8b38-fac9f22cd2fe 61 fields · synced Jun 18, 2026