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PRECICHEK AutoCode AC300

FDA UDI

Class II (US FDA UDI)

by Hmd Biomedical, LLC

Identity

Trade Name
PRECICHEK AutoCode AC300 FDA UDI
Generic Name
Glucose monitoring system IVD, point-of-care FDA UDI
Device Name
PRECICHEK AutoCode AC300 Blood Glucose Mete FDA UDI
Model / Reference
3K-01-16003F FDA UDI
Description
PRECICHEK AutoCode AC300 Blood Glucose Mete FDA UDI

Identifiers

Catalog Number
3K-01-16003F FDA UDI
Primary DI / UDI-DI
04260236850985 FDA UDI
510(k) Number
K120064 FDA UDI
FDA Product Code
NBW 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

PRECICHEK AutoCode AC300 by Hmd Biomedical, 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hmd Biomedical, LLC

Sources (1)

  • FDA UDI fba8769c-3166-4110-9aee-df2c4a487db4 35 fields · synced May 30, 2026