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B-D test package

EUDAMED

Class I (EU MDR)

Ref KBBD

by Jiaxing Kebang Medical Packing Co., Ltd.

Identity

Device Name
B-D test package EUDAMED
Model / Reference
KBBD EUDAMED

Identifiers

Primary DI / UDI-DI
06977341622007 EUDAMED
Basic UDI-DI
697734162PACKAGEVE EUDAMED
EMDN Code
S9099 STERILISATION DEVICES (EXCLUDING CAT. D - Z) - 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: Sterilizer/disinfector rack

B-D test package by Jiaxing Kebang Medical Packing Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Sterilizer/disinfector rack.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000041207
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED e5a4a862-4caa-4d68-9a02-9518db7de7fe 61 fields · synced Jul 29, 2026