MesaLabs

FDA UDI

Class II (US FDA UDI)

by Mesa Laboratories, Inc.

Identity

Trade Name: MesaLabs FDA UDI
Generic Name: Multi-parameter device tester FDA UDI
Device Name: pHoenix XL Dialysate Meter FDA UDI
Model / Reference: 36-00000 FDA UDI
Description: pHoenix XL Dialysate Meter FDA UDI

Identifiers

Catalog Number: 36-00200 FDA UDI
Primary DI / UDI-DI: M98536000000 FDA UDI
FDA Product Code: FIZ FDA UDI
GMDN Term: Multi-parameter device tester FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Multi-parameter device tester

MesaLabs by Mesa Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Mesa Laboratories, Inc.

Sources (1)

FDA UDI af555d85-7ca3-4a92-ae22-e9ceca94a5d5 34 fields · synced May 30, 2026