OneTouch Ultra Plus Flex

FDA UDI

Class II (US FDA UDI)

by Lifescan Europe

Identity

Trade Name: OneTouch Ultra Plus Flex FDA UDI
Generic Name: Glucose monitoring system IVD, home-use FDA UDI
Device Name: OneTouch Ultra Plus Flex™ Blood Glucose Monitoring System FDA UDI
Model / Reference: 024-270 FDA UDI
Description: OneTouch Ultra Plus Flex™ Blood Glucose Monitoring System FDA UDI

Identifiers

Primary DI / UDI-DI: 00353885012621 FDA UDI
FDA Product Code: LFR FDA UDI
NBW 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose monitoring system IVD, home-use

OneTouch Ultra Plus Flex by Lifescan Europe — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Lifescan Europe

Sources (1)

FDA UDI 2e9c60b6-1ef5-4e2f-9b86-c4970a690de7 35 fields · synced Jun 1, 2026