MEDZAH ELBOW SPLINT, MEDIUM

GUDID 10860010472184

Immobilize the elbow, without preventing arm movement. Ideal for covering and protecting arm IV sites. Constructed of nylon laminated foam with reinforced aluminum stays. Hook-and-loop tab closures for easy application and removal. Medium Size.

Medzah Industries

Elbow orthosis

• Primary Device ID: 10860010472184
• NIH Device Record Key: 907fe9ba-bdc0-4023-93e6-8c383797205e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDZAH ELBOW SPLINT, MEDIUM
• Version Model Number: MED-1003
• Company DUNS: 114193536
• Company Name: Medzah Industries
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com
• Phone: 860-288-8696
• Email: info@medzah.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860010472187 [Primary]
GS1	10860010472184 [Package]; Contains: 00860010472187; Package: Case [50 Units]; In Commercial Distribution

FDA Product Code

• IQI: Orthosis, Limb Brace

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: 2024-01-31
• Device Publish Date: 2024-01-23

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