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 |