← Back to catalogue

B-D Test Pack

EUDAMED

Class I (EU MDR)

Ref 15*100mm or customized

by Anqing Kangmingna Packaging Co., Ltd

Identity

Device Name
B-D Test Pack EUDAMED
Model / Reference
15*100mm or customized EUDAMED

Identifiers

Primary DI / UDI-DI
06933401102018 EUDAMED
Basic UDI-DI
69334011KMNBDLZ EUDAMED
EMDN Code
S0199 DEVICES FOR STERILISATION AND PACKAGING (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

B-D Test Pack by Anqing Kangmingna Packaging Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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
CN-MF-000025536
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 3f73a9ad-916e-4997-821b-fb3c00f3962e 61 fields · synced Jul 9, 2026