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Medical Action Industries

FDA UDI

Class II (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Medical Action Industries FDA UDI
Generic Name
Biological sterilization indicator FDA UDI
Model / Reference
SM840 FDA UDI

Identifiers

Primary DI / UDI-DI
20809160002527 FDA UDI
FDA Product Code
LRT 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

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

Medical Action Industries by Medical Action Industries 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

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Manufacturer

Sources (1)

  • FDA UDI c23692cc-1c43-4110-aeee-128ea1166ba9 34 fields · synced May 31, 2026