Primary Device ID | 00863008000126 |
NIH Device Record Key | d47fdc4e-779e-4d62-8e49-108ce835b6bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FemCap |
Version Model Number | 30 mm large |
Catalog Number | 70-399-30 |
Company DUNS | 140036166 |
Company Name | FEMCAP, 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 | false |
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 | true |
OTC Over-The-Counter | false |
Phone | 858-481-8837 |
femcap@yahoo.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00863008000126 [Primary] |
LLQ | Cap, Cervical, Contraceptive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-04-15 |
00863008000126 | FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prev |
00863008000119 | FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prev |
00863008000102 | FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prev |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FEMCAP 75540311 not registered Dead/Abandoned |
Femcap, Inc. 1998-08-21 |
![]() FEMCAP 75231389 not registered Dead/Abandoned |
Helix Medical, Inc. 1997-01-27 |