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Livongo Refill Kit

FDA UDI

Class II (US FDA UDI)

by Livongo Health, Inc

Identity

Trade Name
Livongo Refill Kit FDA UDI
Generic Name
Blood lancing device tip FDA UDI
Device Name
4 bags/pieces Livongo Test Strips, 8 bags/pieces Livongo Sterile Lancets, 1 Instructions for Use (English), 1 Instructions for Use (Spanish) FDA UDI
Model / Reference
200/200 FDA UDI
Description
4 bags/pieces Livongo Test Strips, 8 bags/pieces Livongo Sterile Lancets, 1 Instructions for Use (English), 1 Instructions for Use (Spanish) FDA UDI

Identifiers

Catalog Number
KIT01209 FDA UDI
Primary DI / UDI-DI
00853553005325 FDA UDI
510(k) Number
K133584 FDA UDI
FDA Product Code
FMK 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
862.1345 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

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

Category: Blood lancing device tipGlucose IVD, reagent

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

Similar devices

Also classified as Glucose IVD, reagent.

Cleared under the same submission

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 18b677f7-0a06-4f21-bfdb-7a78fe5af904 36 fields · synced Jun 1, 2026