Primary Device ID | 06937359412397 |
NIH Device Record Key | 29ae470a-c03f-4ef4-837d-489ba94764b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maidwoc |
Version Model Number | M-0232 |
Company DUNS | 527213419 |
Company Name | Wuhan Sitaili Medical Apparatus Development Co., Ltd. |
Device Count | 10 |
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 | false |
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 | 06937359412397 [Unit of Use] |
GS1 | 16937359412394 [Primary] |
FON | Bag, Drainage, With Adhesive, Ostomy |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-27 |
Device Publish Date | 2023-04-19 |
06937359412397 - Maidwoc | 2023-04-27 |
06937359412397 - Maidwoc | 2023-04-27 |
06937359412359 - Steadlive | 2022-12-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAIDWOC 97486587 not registered Live/Pending |
Wuhan Maidewoke Medical Technology Co.,Ltd. 2022-07-01 |