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HardyDisk™

FDA UDI

Class I (US FDA UDI)

by Hardy Diagnostics

Identity

Trade Name
HardyDisk™ FDA UDI
Generic Name
Antibacterial susceptibility testing disc IVD FDA UDI
Device Name
Kanamycin, 1000mcg, differentiates anaerobic bacteria on the basis of susceptibility to kanamycin, 1 x 50 disks, for ID of anaerobes Differentiates anaerobic bacteria on the basis of susceptibility to kanamycin. FDA UDI
Model / Reference
Z7191 FDA UDI
Description
Kanamycin, 1000mcg, differentiates anaerobic bacteria on the basis of susceptibility to kanamycin, 1 x 50 disks, for ID of anaerobes Differentiates anaerobic bacteria on the basis of susceptibility to kanamycin. FDA UDI

Identifiers

Catalog Number
Z7191 FDA UDI
Primary DI / UDI-DI
00816576028450 FDA UDI
FDA Product Code
JTO FDA UDI
GMDN Term
Antibacterial susceptibility testing disc IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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: Antibacterial susceptibility testing disc IVD

HardyDisk™ by Hardy Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antibacterial susceptibility testing disc IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hardy Diagnostics

Sources (1)

  • FDA UDI 371167be-65ae-40c7-b630-76d468234c26 36 fields · synced Jun 1, 2026