IFAK 3331002

GUDID B54133310020

IFAK, custom in drop leg case

FARETEC, INC.

First aid kit, non-medicated, single-use

• Primary Device ID: B54133310020
• NIH Device Record Key: db51e25f-52d7-41c8-b36a-953f8f18489b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IFAK
• Version Model Number: IFAK, Drop Leg
• Catalog Number: 3331002
• Company DUNS: 626802540
• Company Name: FARETEC, 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: false

Customer Support Contacts

• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com
• Phone: 4403509510
• Email: colleen@faretec.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B54133310020 [Primary]

FDA Product Code

• OHO: First Aid Kit Without Drug

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: 2020-09-08
• Device Publish Date: 2020-08-31

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