FemaSeed

GUDID 00859500005103

FemaSeed Intratubal Insemination, FDI-200, 5-Pack

FEMASYS INC.

Assisted reproduction transfer catheter/set
Primary Device ID00859500005103
NIH Device Record Keye733c441-3148-4691-ac57-f644a448f297
Commercial Distribution StatusIn Commercial Distribution
Brand NameFemaSeed
Version Model NumberFDI-200
Company DUNS147590330
Company NameFEMASYS INC.
Device Count5
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100859500005103 [Unit of Use]
GS120859500005107 [Primary]
GS130859500005104 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQFCatheter, Assisted Reproduction

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-01-04
Device Publish Date2023-11-29

On-Brand Devices [FemaSeed]

00859500005011FemaSeed, Intratubal Insemination, 2 pack
10859500005018FemaSeed, Intratubal Insemination, 1 pack
00859500005103FemaSeed Intratubal Insemination, FDI-200, 5-Pack
10859500005100FemaSeed, Intratubal Insemination, 1-Pack

Trademark Results [FemaSeed]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FEMASEED
FEMASEED
88848997 not registered Live/Pending
Femasys Inc.
2020-03-26
FEMASEED
FEMASEED
87203459 not registered Live/Pending
FEMASYS, INC.
2016-10-14
FEMASEED
FEMASEED
85722846 not registered Dead/Abandoned
FEMASYS INC.
2012-09-07

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