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Scan

FDA UDI

Class II (US FDA UDI)

by Lexington Wellness Holdings Inc.

Identity

Trade Name
Scan FDA UDI
Generic Name
Glucose IVD, reagent FDA UDI
Device Name
Blood glucose meter test strips. FDA UDI
Model / Reference
G-427BS FDA UDI
Description
Blood glucose meter test strips. FDA UDI

Identifiers

Primary DI / UDI-DI
00860005561704 FDA UDI
510(k) Number
K191657 FDA UDI
FDA Product Code
CGA FDA UDI
GMDN Term
Glucose IVD, reagent 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose IVD, reagent

Scan by Lexington Wellness Holdings 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

Sources (1)

  • FDA UDI ba412fe9-eb36-4aff-aae3-de0fbd2de6b5 34 fields · synced Jun 8, 2026