The Babydust Method

GUDID 00869220000326

BABYDUST METHOD LLC, THE

Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical

• Primary Device ID: 00869220000326
• NIH Device Record Key: bf6b6c40-56a2-4888-9b9e-bcc5b7c53475
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: The Babydust Method
• Version Model Number: BDW2-S
• Company DUNS: 026887421
• Company Name: BABYDUST METHOD LLC, THE
• 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: false
• 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

Customer Support Contacts

• Phone: 3103876976
• Email: babydustmethod@gmail.com
• Phone: 3103876976
• Email: babydustmethod@gmail.com
• Phone: 3103876976
• Email: babydustmethod@gmail.com
• Phone: 3103876976
• Email: babydustmethod@gmail.com
• Phone: 3103876976
• Email: babydustmethod@gmail.com
• Phone: 3103876976
• Email: babydustmethod@gmail.com
• Phone: 3103876976
• Email: babydustmethod@gmail.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00869220000326 [Primary]

FDA Product Code

• CEP: Radioimmunoassay, Luteinizing Hormone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-06-10
• Device Publish Date: 2020-07-14

On-Brand Devices [The Babydust Method]

• 00869220000302: BDW1-S
• 00869220000326: BDW2-S