e.p.t. Analog

GUDID 00045611952027

e.p.t. Analog 2 Ct

Nfi Consumer Products

Total human chorionic gonadotropin (HCG) IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 00045611952027
• NIH Device Record Key: a7ab00d8-715e-4361-98c8-a2d6ff7886f8
• Commercial Distribution Discontinuation: 2018-01-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: e.p.t. Analog
• Version Model Number: ept analog
• Company DUNS: 016785052
• Company Name: Nfi Consumer Products
• Device Count: 2
• DM Exempt: false
• Pre-market Exempt: false
• 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: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com
• Phone: 1-800-3781783
• Email: customerservice@nficorporate.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00045611952027 [Primary]
GS1	80045611952023 [Unit of Use]

FDA Product Code

• LCX: Kit, Test, Pregnancy, Hcg, Over The Counter

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-02-19
• Device Publish Date: 2017-09-25

Devices Manufactured by Nfi Consumer Products

• 00045611953031 - e.p.t. Early Pregnancy Test: 2023-07-06 ept analog 3 Ct
• 00045611962026 - e.p.t. Direct: 2023-07-06 e.p.t. Direct 2 ct.
• 00045611963030 - e.p.t. Direct: 2023-07-06 e.p.t. Direct 3 ct.
• 00045611952027 - e.p.t. Analog: 2020-02-19e.p.t. Analog 2 Ct
• 00045611952027 - e.p.t. Analog: 2020-02-19 e.p.t. Analog 2 Ct