FemCerv 03140

GUDID 10859500005056

FemCerv, Endocervical Sampler, 13 Fr, 1-pack

FEMASYS INC.

Cervical cytology brush

• Primary Device ID: 10859500005056
• NIH Device Record Key: 8b37f625-fb64-4291-8657-a4a1ba827007
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FemCerv
• Version Model Number: FCV-013
• Catalog Number: 03140
• Company DUNS: 147590330
• Company Name: FEMASYS 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	10859500005056 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122658

FDA Product Code

• PCF: Sampler, Endocervical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-29
• Device Publish Date: 2022-09-21

On-Brand Devices [FemCerv]

• 00859500005066: FemCerv, Endocervical Sampler, 11 Fr, 10-pack
• 00859500005059: FemCerv, Endocervical Sampler, 13 Fr, 10-pack
• 10859500005063: FemCerv, Endocervical Sampler, 11 Fr, 1-pack
• 10859500005056: FemCerv, Endocervical Sampler, 13 Fr, 1-pack