Jigsaw Medical,LLC KT101

GUDID 00856274008514

Kinesiology Tape - Black

JIGSAW MEDICAL, LLC

Pressure bandage, non-latex, non-sterile, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use

• Primary Device ID: 00856274008514
• NIH Device Record Key: 3ab3c7ec-3b10-4458-a640-1e8601f6af31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jigsaw Medical,LLC
• Version Model Number: KT101
• Catalog Number: KT101
• Company DUNS: 079233827
• Company Name: JIGSAW MEDICAL, LLC
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856274008507 [Primary]
GS1	00856274008514 [Package]; Contains: 00856274008507; Package: Case [2 Units]; In Commercial Distribution

FDA Product Code

• KGX: Tape And Bandage, Adhesive

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: 2019-12-17
• Device Publish Date: 2019-12-09

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