← Back to catalogue

3M™ Attest™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Attest™ FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
3M™ Attest™ Steam Chemical Integrator Test Pack, 41360, 4 PK/BG 4 BG/BX 4 BX/CS FDA UDI
Model / Reference
41360 FDA UDI
Description
3M™ Attest™ Steam Chemical Integrator Test Pack, 41360, 4 PK/BG 4 BG/BX 4 BX/CS FDA UDI

Identifiers

Catalog Number
41360 FDA UDI
Primary DI / UDI-DI
30707387787241 FDA UDI
FDA Product Code
FRC FDA UDI
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

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

Category: Chemical/physical sterilization process indicator

3M™ Attest™ by 3m Company — 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

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

Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 5050b568-9cec-4d1f-9305-bf783a89eaba 35 fields · synced May 30, 2026