3M™ Steri-Drape™ Cardiovascular Sheet with Ioban™ 6681

GUDID 10707387815599

3M™ Steri-Drape™ Cardiovascular Sheet with Ioban™ 2 Incise Film, 6681, 1/CS

3M COMPANY

Patient surgical drape, single-use
Primary Device ID10707387815599
NIH Device Record Keyebbd6523-4e04-47cd-972c-b2a28faa0772
Commercial Distribution StatusIn Commercial Distribution
Brand Name3M™ Steri-Drape™ Cardiovascular Sheet with Ioban™
Version Model Number6681
Catalog Number6681
Company DUNS830016148
Company Name3M COMPANY
Device Count8
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

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
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
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
GS110707387815599 [Unit of Use]
GS150707387815597 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KKXDrape, surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-08-20
Device Publish Date2024-08-12

Devices Manufactured by 3M COMPANY

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50707387815566 - 3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™2024-09-23 3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 2 Incise Film and Clear Screen, 6697CA, 5/CS
50707387814583 - 3M™2024-08-27 3M™ Surgical Clipper with Pivoting Head, 9661L, 1 Each/Case
50707387814590 - 3M™2024-08-27 3M™ Surgical Clipper with Pivoting Head, 9667L, 1/Case
50707387814606 - 3M™2024-08-27 3M™ Surgical Clipper Starter Kit (9661L Clipper and 9663L Charger Stand) 9667L-A
50707387814613 - 3M™2024-08-27 3M™ Surgical Clipper Starter Kit (9661L Clipper and 9668L Charger Stand) 9667L-E
00707387000011 - Red Dot™2024-08-23 3M™ Red Dot™ Trace Prep 2236

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