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Rubber Bulb

EUDAMED

Class I (EU MDR)

Ref 70-522

by Hospital Equipment Mfg. Co.

Identity

Device Name
Rubber Bulb EUDAMED
Model / Reference
70-522 EUDAMED

Identifiers

Primary DI / UDI-DI
00860004277385 EUDAMED
Basic UDI-DI
0860007128670-522XR EUDAMED
Direct Marketing DI
00860004277385 EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Rubber Bulb by Hospital Equipment Mfg. Co. — 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
IN-MF-000017056
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED c96474b5-cf8d-4cbc-86cc-f9ab6b5e93fd 61 fields · synced Jul 11, 2026