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Fingertip Pulse Oximeter

EUDAMED

Class IIa (EU MDR)

Ref YM402Model YM101, YM102, YM103, YM104, YM201, YM202, YM301, YM302, YM111, YM112, YM113, YM114, YM211, YM212, YM314, YM401, YM402, YM403, YM501, YM502, YM503, YM504, YM601, YM602, YM603

by Shenzhen Yimi Life Technology Co., Ltd

Identity

Trade Name
Fingertip Pulse Oximeter EUDAMED
Device Name
Fingertip Pulse Oximeter EUDAMED
Model / Reference
YM101, YM102, YM103, YM104, YM201, YM202, YM301, YM302, YM111, YM112, YM113, YM114, YM211, YM212, YM314, YM401, YM402, YM403, YM501, YM502, YM503, YM504, YM601, YM602, YM603 EUDAMED
YM402 EUDAMED

Identifiers

Primary DI / UDI-DI
06972911370227 EUDAMED
Basic UDI-DI
697291137YM4A EUDAMED
Direct Marketing DI
06972911370227 EUDAMED
EMDN Code
Z1203020408 PULSE OXIMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Fingertip Pulse Oximeter by Shenzhen Yimi Life- Technology Co.ltd — Class IIa — 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-000029928
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED c1a3441e-0e99-4d4b-8c35-c954d5ac1093 61 fields · synced Jun 18, 2026