Primary Device ID | 06941917833173 |
NIH Device Record Key | 80e54db8-caa5-47f3-a83b-0e2989d1b0da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lorski |
Version Model Number | 3×5cm |
Company DUNS | 554551139 |
Company Name | Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06941917833173 [Primary] |
MDA | Elastomer, Silicone, For Scar Management |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-25 |
Device Publish Date | 2024-12-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LORSKI 90156669 not registered Live/Pending |
ELYRADIA BIOTECHNOLOGY LIMITED 2020-09-03 |