3M™ Attest™ 41382F

GUDID 50707387787269

3M™ Attest™ Rapid 5 Steam-Plus Test Packs, 41382F, 16 packs / box, 4 boxes / case

3M COMPANY

Biological sterilization indicator
Primary Device ID50707387787269
NIH Device Record Keydac6c173-018e-4c37-8ac3-265ff3f6bda3
Commercial Distribution StatusIn Commercial Distribution
Brand Name3M™ Attest™
Version Model Number41382F
Catalog Number41382F
Company DUNS830016148
Company Name3M COMPANY
Device Count16
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100707387787257 [Unit of Use]
GS130707387787265 [Primary]
GS150707387787269 [Package]
Contains: 30707387787265
Package: BOX [4 Units]
In Commercial Distribution

FDA Product Code

FRCIndicator, biological sterilization process

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-08-31
Device Publish Date2021-08-23

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507073877872693M™ Attest™ Rapid 5 Steam-Plus Test Packs, 41382F, 16 packs / box, 4 boxes / case
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507073877872453M™ Attest™ Steam Chemical Integrator Test Pack, 41360, 4 PK/BG 4 BG/BX 4 BX/CS
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