3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 6697CA

GUDID 50707387815566

3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™ 2 Incise Film and Clear Screen, 6697CA, 5/CS

3M COMPANY

Patient surgical drape, single-use
Primary Device ID50707387815566
NIH Device Record Keye3f6fae9-0121-43d4-a376-b1a4fd75cf21
Commercial Distribution StatusIn Commercial Distribution
Brand Name3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™
Version Model Number6697CA
Catalog Number6697CA
Company DUNS830016148
Company Name3M COMPANY
Device Count1
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 Datetrue
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
GS110707387815568 [Primary]
GS150707387815566 [Package]
Contains: 10707387815568
Package: CV [5 Units]
In Commercial Distribution

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 Date2024-09-23
Device Publish Date2024-09-13

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