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microdot Blood Glucose Test Strips

FDA UDI

Class II (US FDA UDI)

by Cambridge Sensors Limited

Identity

Trade Name
microdot Blood Glucose Test Strips FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
microdot Blood gucose test strips for use with micodot Blood glucose meter FDA UDI
Model / Reference
100-50 FDA UDI
Description
microdot Blood gucose test strips for use with micodot Blood glucose meter FDA UDI

Identifiers

Primary DI / UDI-DI
05060141250035 FDA UDI
510(k) Number
K070524 FDA UDI
FDA Product Code
LFR FDA UDI
GMDN Term
Glucose monitoring system IVD, home-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose monitoring system IVD, home-use

microdot Blood Glucose Test Strips by Cambridge Sensors Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1eb69ab4-9898-47c4-9290-2413a3196314 35 fields · synced May 29, 2026