AccessGUDID - DEVICE: Anscare LeniScar Silicone Stick (14719745020879)

GUDID

Device Identifier (DI) Information

Brand Name: Anscare LeniScar Silicone Stick
Version or Model: SP-14-1112
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: BENQ MATERIALS CORP.

Primary DI Number: 14719745020879
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 657476292 *Terms of Use

Device Description: Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended to diminish hypertrophic scars and keloids characterized with a raised or discolored appearance. LeniScar is an advanced silicone formula which contains medical grade silicone and antioxidant vitamin C & E. It creates a waterproof, transparent thin film which helps to maintain the moisture balance of skin and provides an optimal protective barrier for the scar to restore.

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":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	Yes
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?
44898	Scar-management dressing, reusable	A covering made of, or coated with, a synthetic polymer material (e.g., silicone gel) intended to be applied directly to the skin for the management of hypertrophic or keloid scars. The device is typically in the form of an elastic sheet that occludes the skin to hydrate and reduce red, dark, or raised scars resulting from surgery, accidents, cuts, burns, or other injuries. The device may be self-adhesive or fixed by tape; it may be washable. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MDA	Elastomer, Silicone, For Scar Management

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
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: 2bf463c8-77d2-4305-8aa2-19f0b7516361
Public Version Date: February 16, 2024
Public Version Number: 2
DI Record Publish Date: September 19, 2022