← Back to catalogue

CareSens N

FDA UDI

Class II (US FDA UDI)

by i-SENS, Inc.

Identity

Trade Name
CareSens N FDA UDI
Generic Name
Home-use/point-of-care glucose analyser IVD, battery-powered FDA UDI
Device Name
CareSens N Blood Glucose Meter FDA UDI
Model / Reference
164301-202 FDA UDI
Description
CareSens N Blood Glucose Meter FDA UDI

Identifiers

Primary DI / UDI-DI
00885325000115 FDA UDI
510(k) Number
K083468 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Home-use/point-of-care glucose analyser IVD, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Home-use/point-of-care glucose analyser IVD, battery-powered

CareSens N by i-SENS, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use/point-of-care glucose analyser IVD, battery-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
i-SENS, Inc.

Sources (1)

  • FDA UDI 94b57f93-836c-4217-9164-221c2941bcfa 36 fields · synced May 29, 2026