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In Touch Refill Kit

FDA UDI

Class II (US FDA UDI)

by Livongo Health, Inc

Identity

Trade Name
In Touch Refill Kit FDA UDI
Generic Name
Blood lancing device tip FDA UDI
Device Name
6 boxes of In Touch Test Strips, 1 box of In Touch Lancets, 1 box of In Touch high/low Control Solution FDA UDI
Model / Reference
In Touch FDA UDI
Description
6 boxes of In Touch Test Strips, 1 box of In Touch Lancets, 1 box of In Touch high/low Control Solution FDA UDI

Identifiers

Catalog Number
KIT00147 FDA UDI
Primary DI / UDI-DI
00853553005103 FDA UDI
FDA Product Code
FMK FDA UDI
JJX FDA UDI
CGA FDA UDI
GMDN Term
Blood lancing device tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 FDA UDI
862.1660 FDA UDI
862.1345 FDA UDI
Commercial Distribution
Not 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

Yes

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

In Touch Refill Kit by Livongo Health, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Livongo Health, Inc

Sources (1)

  • FDA UDI 2a519b60-696d-4dcf-87e3-68baa903f3ea 37 fields · synced Jun 1, 2026