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Steamplus Sterilization Integrator

FDA UDI

Class II (US FDA UDI)

by Spsmedical Supply Corp.

Identity

Trade Name
STEAMPLUS STERILIZATION INTEGRATOR FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
Wicking-style device that verifies when all critical parameters of steam sterilization have been met during a sterilizer cycle. FDA UDI
Model / Reference
SSI-250 FDA UDI
Description
Wicking-style device that verifies when all critical parameters of steam sterilization have been met during a sterilizer cycle. FDA UDI

Identifiers

Catalog Number
SSI-250 FDA UDI
Primary DI / UDI-DI
10732224710805 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Chemical/physical sterilization process indicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

Yes

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

Category: Chemical/physical sterilization process indicator

Steamplus Sterilization Integrator by Spsmedical Supply Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemical/physical sterilization process indicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spsmedical Supply Corp.

Sources (1)

  • FDA UDI 56956e6c-8a2e-46b5-8e6d-5246e7fb31f7 36 fields · synced Jun 6, 2026