Primary Device ID | 14719745020879 |
NIH Device Record Key | 2bf463c8-77d2-4305-8aa2-19f0b7516361 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anscare LeniScar Silicone Stick |
Version Model Number | SP-14-1112 |
Company DUNS | 657476292 |
Company Name | BENQ MATERIALS CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 14719745020879 [Primary] |
MDA | Elastomer, Silicone, For Scar Management |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-27 |
Device Publish Date | 2022-09-19 |
14719745020879 | Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended t |
14719745020855 | Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended t |
04719745505058 | Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended t |
04719745504525 | Anscare Leniscar Silicone Stick provides an easy-to-use topical scar treatment. It is intended t |