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EarlySense® InSight™

FDA UDI

Class II (US FDA UDI)

by Earlysense, Ltd.

Identity

Trade Name
EarlySense® InSight™ FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Model / Reference
Insight at Home FDA UDI

Identifiers

Catalog Number
AME-02021 FDA UDI
Primary DI / UDI-DI
07290016169393 FDA UDI
510(k) Number
K152911 FDA UDI
FDA Product Code
BZQ FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose multi-parameter bedside monitor

EarlySense® InSight™ by Earlysense, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Cleared under the same submission

K152911 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Earlysense, Ltd.

Sources (1)

  • FDA UDI cc5d00a9-6cca-46f2-993e-604e33d9c8ae 34 fields · synced May 30, 2026