Primary Device ID | 30859500005166 |
NIH Device Record Key | 84df52d0-6af0-4bf8-936a-97cd76faa7da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | StopLock |
Version Model Number | SLK-100 |
Catalog Number | 04392 |
Company DUNS | 147590330 |
Company Name | FEMASYS INC. |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859500005165 [Unit of Use] |
GS1 | 30859500005166 [Primary] |
PTM | Syringe, Balloon Inflation, Exempt |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-12 |
Device Publish Date | 2025-05-02 |
30859500005166 | StopLock Balloon Inflation Syringe 10-Pack, SLK-100 |
00859500005165 | StopLock Balloon Inflation Syringe 5-Pack, SLK-100 |
10859500005162 | StopLock Balloon Inflation Syringe 1-Pack , SLK-100 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() STOPLOCK 97088419 not registered Live/Pending |
Femasys Inc. 2021-10-22 |
![]() STOPLOCK 75178321 2101508 Dead/Cancelled |
PC Security Limited 1996-09-23 |
![]() STOPLOCK 75170326 2133973 Dead/Cancelled |
PC Security Limited 1996-09-23 |
![]() STOPLOCK 74290717 not registered Dead/Abandoned |
HOMER ENTERPRISE CO., LTD. 1992-07-02 |
![]() STOPLOCK 73516273 1375596 Dead/Cancelled |
SDI INCORPORATED 1985-01-07 |