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MesaLabs

FDA UDI

Class I (US FDA UDI)

by Mesa Laboratories, Inc.

Identity

Trade Name
MesaLabs FDA UDI
Generic Name
pH-adjusted buffer solution IVD FDA UDI
Device Name
Standard Buffer Solution 4.00 pH 16 oz. FDA UDI
Model / Reference
02.0032 FDA UDI
Description
Standard Buffer Solution 4.00 pH 16 oz. FDA UDI

Identifiers

Catalog Number
02.0032 FDA UDI
Primary DI / UDI-DI
M9850200320 FDA UDI
FDA Product Code
JCC FDA UDI
GMDN Term
pH-adjusted buffer solution IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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: pH-adjusted buffer solution IVD

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

Similar devices

Also classified as pH-adjusted buffer solution IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 47d58316-e091-4f8e-a649-5f53e1cfce88 34 fields · synced Jun 8, 2026