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MED-62 Aneroid Blood Pressure Kit

EUDAMED

Class I (EU MDR)

Ref 1101323Model MED-61, MED-62, MED-63, PRO-60

by B.Well Swiss AG

Identity

Trade Name
MED-62 Aneroid Blood Pressure Kit EUDAMED
Device Name
Aneroid Blood Pressure Kit EUDAMED
Model / Reference
MED-61, MED-62, MED-63, PRO-60 EUDAMED
1101323 EUDAMED

Identifiers

Primary DI / UDI-DI
07640156395938 EUDAMED
Basic UDI-DI
764015639MDN1207_1U7 EUDAMED
Direct Marketing DI
07640156395938 EUDAMED
EMDN Code
C9006 ANEROID SPHYGMOMANOMETERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

MED-62 Aneroid Blood Pressure Kit by B.Well Swiss AG — 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

Manufacturer
B.Well Swiss AG
EUDAMED SRN
CH-MF-000012588
Authorised Representative
Blue Broccoli GmbH LI-AR-000000233

Sources (1)

  • EUDAMED b15ca517-c994-4010-b913-5c112ebc3889 61 fields · synced Jul 12, 2026