AccessGUDID - DEVICE: 3M™ Cavilon™ (30707387498536)

GUDID

Device Identifier (DI) Information

Brand Name: 3M™ Cavilon™
Version or Model: 3344E
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 3344E
Company Name: 3M COMPANY

Primary DI Number: 30707387498536
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 30
Labeler D-U-N-S® Number*: 830016148 *Terms of Use

Device Description: 3M™ Cavilon™ No Sting Barrier Film, 3344E, 1ML Wipe, 30 Each/Carton, 6 Cartons/Case

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
58979	Synthetic-polymer liquid barrier dressing, sterile	A sterile liquid preparation composed of synthetic polymer materials intended to form a thin protective film when applied to superficial wounds (e.g., minor cuts, abrasions) and/or intact skin (typically sensitive areas such as around a stoma), to reduce exposure to external contaminants; may also be intended to augment the adherence of medical adhesives, or provide a protective interface when removing medical adhesives. It may be presented as a wipe, swab, or spray. After application, this device cannot be reused.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
KMF	Bandage, liquid

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K955103	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 7e263bf8-0d12-4ca2-867c-eeb31714d7a3
Public Version Date: December 16, 2022
Public Version Number: 1
DI Record Publish Date: December 08, 2022