| 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 |