ivWatch Sensor Receptacle

by ivWatch, LLC

Ref AM-1002074Model Model 400

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number081408802AM-1002074SZ Basic UDI-DI 00814088020863UDI-DI	Date24 Oct 2022Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: Model 400, AM-1002074

Primary DI / UDI-DI: 00814088020863
Basic UDI-DI: 081408802AM-1002074SZ
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: US-MF-000001531
Authorised representative: Emergo Europe B.V. NL-AR-000000116

Other devices from Ivwatch, LLC

ivWatch Patient Monitor Model 400

Class II
ivWatch SmartTouch Sensor Model 400

Class II
ivWatch Sensor Receptacle Model 400

Class II
ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable

Class II
ivWatch Fiber Optic Sensor Cable

Class I
ivWatch Patient Monitor

Class IIa

See all devices from Ivwatch, LLC →

Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No