Primary Device ID | 06934184004445 |
NIH Device Record Key | ef4901da-e9f5-488c-99c6-77d0350d0b94 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MultiStage® |
Version Model Number | MSO-1555-23 |
Company DUNS | 551476865 |
Company Name | Dongguan TT Medical, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 06934184004445 [Primary] |
FGE | Stents, Drains And Dilators For The Biliary Ducts |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-18 |
Device Publish Date | 2025-02-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MULTISTAGE 79068409 3734489 Dead/Cancelled |
Samsung Electronics Co., Ltd. 2008-12-08 |
![]() MULTISTAGE 79059654 3692749 Dead/Cancelled |
Samsung Electronics Co., Ltd. 2008-07-04 |
![]() MULTISTAGE 75797071 not registered Dead/Abandoned |
Ancor Communications, Inc. 1999-09-10 |