← Back to catalogue

OneTouch Ultra Blue

FDA UDI

Class II (US FDA UDI)

by Lifescan Europe

Identity

Trade Name
OneTouch Ultra Blue FDA UDI
Generic Name
Glucose IVD, kit, electrometry FDA UDI
Device Name
OneTouch Ultra Test Strips Blue for blood glucose testing with: OneTouch Ultra 2, OneTouch UltraMini, OneTouch Ultra, OneTouch UltraSmart, OneTouch Ping and OneTouch UltraLink Meters FDA UDI
Model / Reference
020-963 FDA UDI
Description
OneTouch Ultra Test Strips Blue for blood glucose testing with: OneTouch Ultra 2, OneTouch UltraMini, OneTouch Ultra, OneTouch UltraSmart, OneTouch Ping and OneTouch UltraLink Meters FDA UDI

Identifiers

Catalog Number
020-963 FDA UDI
Primary DI / UDI-DI
00353885004183 FDA UDI
FDA Product Code
NBW FDA UDI
CGA 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, kit, electrometry

OneTouch Ultra Blue 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

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

Manufacturer

Manufacturer
Lifescan Europe

Sources (1)

  • FDA UDI eb86d4c4-9a92-4aa1-8054-64d3ab25d8a7 36 fields · synced Jun 8, 2026