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One Drop

FDA UDI

Class II (US FDA UDI)

by Informed Data Systems Inc.

Identity

Trade Name
One Drop FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
Blood Glucose Meter, One Drop, mg/dL FDA UDI
Model / Reference
8000-10465 FDA UDI
Description
Blood Glucose Meter, One Drop, mg/dL FDA UDI

Identifiers

Primary DI / UDI-DI
00859509006019 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose monitoring system IVD, home-use 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose monitoring system IVD, home-use

One Drop by Informed Data Systems Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9a45f453-3c8d-4e96-9153-54f3c35c0789 34 fields · synced May 31, 2026