← Back to catalogue

ProSpore2

FDA UDI

Class II (US FDA UDI)

by Mesa Laboratories, Inc.

Identity

Trade Name
ProSpore2 FDA UDI
Generic Name
Biological sterilization indicator FDA UDI
Device Name
Self-contained biological indicator for use in steam sterilization, 10e6 population, 50-count box FDA UDI
Model / Reference
10e6 FDA UDI
Description
Self-contained biological indicator for use in steam sterilization, 10e6 population, 50-count box FDA UDI

Identifiers

Catalog Number
PS2-3-6-50 FDA UDI
Primary DI / UDI-DI
M985PS236501 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Biological sterilization indicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

ProSpore2 by Mesa Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 58cf5217-d7f4-4278-99a1-14617f46c85f 35 fields · synced Jun 8, 2026