Primary Device ID | 06938799200131 |
NIH Device Record Key | 9054bef8-be5b-4207-b9ea-32450a5e7795 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | wemade |
Version Model Number | 5CM X 450CM |
Company DUNS | 549550760 |
Company Name | Wuxi Wemade Healthcare Products Co.,Ltd. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06938799200131 [Primary] |
FQM | Bandage, Elastic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-14 |
Device Publish Date | 2023-03-06 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() WEMADE 98262025 not registered Live/Pending |
Anhui Weimeide leisure products Co., LTD 2023-11-09 |
![]() WEMADE 97075603 not registered Live/Pending |
HENGLYÂ ASSOCIATESÂ INC. 2021-10-14 |
![]() WEMADE 79264553 not registered Live/Pending |
Wemade Entertainment Co., Ltd. 2019-05-07 |