| Primary Device ID | 00859500005127 |
| NIH Device Record Key | f8ce0200-2050-4b2a-a0f9-337b0d5c75c1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VariLock |
| Version Model Number | VL-1001 |
| Catalog Number | 04178 |
| Company DUNS | 147590330 |
| Company Name | FEMASYS INC. |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00859500005127 [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 | 2024-03-21 |
| Device Publish Date | 2024-03-13 |
| 00859500005073 | VariLock Balloon Inflation Syringe, Bulk Sterile |
| 00859500005127 | VariLock Balloon Inflation Syringe 3mL, Bulk Sterile |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VARILOCK 98596716 not registered Live/Pending |
Femsys Inc. 2024-06-12 |
![]() VARILOCK 97697973 not registered Live/Pending |
Femasys Inc. 2022-11-30 |
![]() VARILOCK 77303877 3674999 Dead/Cancelled |
CHROSZIEL GmbH 2007-10-15 |
![]() VARILOCK 75750839 not registered Dead/Abandoned |
OSSUR H.F. 1999-07-14 |