Primary Device ID | 06938799233238 |
NIH Device Record Key | d9b9b6e1-bcc6-4d5a-b87d-cbe248508803 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wemade |
Version Model Number | 3323 |
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 | true |
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 | 06938799233238 [Primary] |
KGX | Tape And Bandage, Adhesive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-27 |
Device Publish Date | 2025-03-19 |
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 |