Mueller Medi Kit Refill 200750

GUDID 00074676207506

MEDI KIT REFILL KIT

Mueller Sports Medicine, Inc.

First aid kit, medicated

• Primary Device ID: 00074676207506
• NIH Device Record Key: fa1a630f-68e7-4f11-a4f4-ef062d9b58fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mueller Medi Kit Refill
• Version Model Number: 200750
• Catalog Number: 200750
• Company DUNS: 006426316
• Company Name: Mueller Sports Medicine, Inc.
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com
• Phone: +1(608)643-8530
• Email: Regulatory@muellersportsmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00074676207506 [Primary]

FDA Product Code

• LRR: First Aid Kit with 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: 2022-09-08
• Device Publish Date: 2022-08-31

Devices Manufactured by Mueller Sports Medicine, Inc.

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• 80074676004088 - MUELLER KINSIOLOGY EASY FIT PRE-CUT NECK: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT NECK BK
• 80074676004095 - MUELLER KINSIOLOGY EASY FIT PRE-CUT ARCH: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT ARCH BK
• 80074676004101 - MUELLER KINESIOLOGY EASY FIT PRE-CUT CALF/ANKLE TAPE: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT CALF/ANKLE
• 80074676004118 - MUELLER KINESIOLOGY EASY FIT PRE-CUT BK: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT KNEE BK
• 80074676004125 - MUELLER KINESIOLOGY EASY FIT PRE-CUT WAIST/BACK: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT WAIST/BACK
• 80074676004132 - MUELLER KINESIOLOGY EAST FIT PRE-CUT SHOULDER: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT SHOULDER BK
• 80074676004149 - MUELLER KINESIOLOGY EASY FIT PRE-CUT X PATTERN: 2022-10-24 KINESIOLOGY EASY FIT PRE-CUT X PATTERN