← Back to catalogue

Fresh Test

FDA UDI

Class II (US FDA UDI)

by Fresh Test, LLC

Identity

Trade Name
Fresh Test FDA UDI
Generic Name
Glucose monitoring system IVD, point-of-care FDA UDI
Device Name
Fresh Test 50g Beverage Glucose Tolerance Test FDA UDI
Model / Reference
Beverage 50 Gram FDA UDI
Description
Fresh Test 50g Beverage Glucose Tolerance Test FDA UDI

Identifiers

Catalog Number
27102050 FDA UDI
Primary DI / UDI-DI
G219271020501 FDA UDI
FDA Product Code
MRV FDA UDI
GMDN Term
Glucose monitoring system IVD, point-of-care 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose monitoring system IVD, point-of-care

Fresh Test by Fresh Test, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, point-of-care.

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
Fresh Test, LLC

Sources (1)

  • FDA UDI 54bdd9ce-03e4-4602-8749-e07277db4137 34 fields · synced May 30, 2026