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Infant Flex Sensor

EUDAMED

Class IIb (EU MDR)

Ref 0740-000Model MODEL 8008J, INFANT FLEX SENSOR

by Nonin Medical, Inc.

Identity

Trade Name
Infant Flex Sensor EUDAMED
Device Name
Infant Flex Sensor EUDAMED
Model / Reference
MODEL 8008J, INFANT FLEX SENSOR EUDAMED
0740-000 EUDAMED

Identifiers

Primary DI / UDI-DI
00833166000610 EUDAMED
Basic UDI-DI
B-00833166000610 EUDAMED
EMDN Code
C900301 PULSE OXIMETER SENSORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Pulse oximeter probe, single-use

Infant Flex Sensor by Nonin Medical, Inc. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Nonin Medical, Inc.
EUDAMED SRN
US-MF-000008228
Authorised Representative
MPS Medical Product Service GmbH DE-AR-000005009

Sources (1)

  • EUDAMED ca975b94-f3e9-464c-aae2-04851bb277c6 61 fields · synced Jun 18, 2026