Proov

GUDID 00850035206058

At home IVD FSH test to measure follicle stimulating hormone and check your ovarian reserve status.

Mfb Fertility, Inc.

Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing

• Primary Device ID: 00850035206058
• NIH Device Record Key: 3c1d6508-b050-4c1b-b7d9-60aa3f0407f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Proov
• Version Model Number: Reserve
• Company DUNS: 080270263
• Company Name: Mfb Fertility, 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: true
• 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: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850035206058 [Primary]

FDA Product Code

• NGA: Test, Follicle Stimulating Hormone (Fsh), Over The Counter

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-25
• Device Publish Date: 2023-04-17

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