Curaplex 8600-01405

GUDID 00851772007335

*Custom* Lycoming County Public IFAK Advanced

EMERGENCY MEDICAL PRODUCTS, INC.

First aid kit, non-medicated, reusable

• Primary Device ID: 00851772007335
• NIH Device Record Key: 6757ac7f-2db8-4539-8115-c54024b3b2e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaplex
• Version Model Number: 8600-01405
• Catalog Number: 8600-01405
• Company DUNS: 061738290
• Company Name: EMERGENCY MEDICAL PRODUCTS, 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851772007335 [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: 2019-09-09
• Device Publish Date: 2019-08-30

On-Brand Devices [Curaplex]

• 00851772007335: *Custom* Lycoming County Public IFAK Advanced
• 00851772007328: *Custom* Lycoming County Public IFAK Basic