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Livongo Replacement Device

FDA UDI

Class II (US FDA UDI)

by Livongo Health, Inc

Identity

Trade Name
Livongo Replacement Device FDA UDI
Generic Name
Home-use/point-of-care glucose analyser IVD, battery-powered FDA UDI
Device Name
Livongo Blood Glucose Meter BG300, Charger, Charger Cable, 1 User Guide (English), 1 User Guide (Spanish) FDA UDI
Model / Reference
Livongo FDA UDI
Description
Livongo Blood Glucose Meter BG300, Charger, Charger Cable, 1 User Guide (English), 1 User Guide (Spanish) FDA UDI

Identifiers

Catalog Number
KIT00423 FDA UDI
Primary DI / UDI-DI
00853553005240 FDA UDI
510(k) Number
K133584 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Home-use/point-of-care glucose analyser IVD, battery-powered 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

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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Home-use/point-of-care glucose analyser IVD, battery-powered

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

Similar devices

Also classified as Home-use/point-of-care glucose analyser IVD, battery-powered.

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 6f56fcc3-1cdf-4c30-bd35-fe7455ba6e98 37 fields · synced Jun 8, 2026