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aneroid sphygmomanometer

EUDAMED

Class I (EU MDR)

Ref BK2006Model BK2001, BK2002, BK2005, BK2001-3001, BK2001-3002, BK2001-3003, BK2003, BK2004, BK2009, BK2099, BK2015, BK2012, BK2066, BK2006, BK2007

by Wenzhou Bokang Instruments Co., Ltd

Identity

Trade Name
aneroid sphygmomanometer EUDAMED
Device Name
aneroid sphygmomanometer EUDAMED
Model / Reference
BK2001, BK2002, BK2005, BK2001-3001, BK2001-3002, BK2001-3003, BK2003, BK2004, BK2009, BK2099, BK2015, BK2012, BK2066, BK2006, BK2007 EUDAMED
BK2006 EUDAMED

Identifiers

Primary DI / UDI-DI
06931038620608 EUDAMED
Basic UDI-DI
69310386ANE001BP EUDAMED
EMDN Code
C9006 ANEROID SPHYGMOMANOMETERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

aneroid sphygmomanometer by Wenzhou Bokang Instruments 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

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Manufacturer

EUDAMED SRN
CN-MF-000021505
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ae0b733d-f17a-4613-93b5-b27c864f9c4e 61 fields · synced May 23, 2026