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OneTouch Ultra Plus

FDA UDI

Class II (US FDA UDI)

by Lifescan Europe

Identity

Trade Name
OneTouch Ultra Plus FDA UDI
Generic Name
Glucose IVD, kit, electrometry FDA UDI
Device Name
OneTouch Ultra® Plus strips work with OneTouch Ultra Plus Flex(TM) meter. FDA UDI
Model / Reference
024-271 FDA UDI
Description
OneTouch Ultra® Plus strips work with OneTouch Ultra Plus Flex(TM) meter. FDA UDI

Identifiers

Primary DI / UDI-DI
00353885012638 FDA UDI
FDA Product Code
LFR FDA UDI
NBW FDA UDI
GMDN Term
Glucose IVD, kit, electrometry 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 IVD, kit, electrometry

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

Similar devices

Also classified as Glucose IVD, kit, electrometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lifescan Europe

Sources (1)

  • FDA UDI 4fd5abb9-a396-4a69-ac29-53bbc3a66d4f 35 fields · synced May 31, 2026