Phase 4 Gel® 509-P4-NSP.1

GUDID 00696588005621

Sample Phase 4 Gel® Splint - Non Sterile (1 each)

Innovative Medical Products, Inc

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• Primary Device ID: 00696588005621
• NIH Device Record Key: b3a40c45-3f74-4ead-8ad8-27cd587839d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phase 4 Gel®
• Version Model Number: 509-P4-NSP.1
• Catalog Number: 509-P4-NSP.1
• Company DUNS: 147363154
• Company Name: Innovative Medical Products, 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: false
• Device Combination Product: false
• Single Use: true
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00696588005621 [Primary]

FDA Product Code

• FMP: Protector, Skin Pressure

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: 2022-08-10
• Device Publish Date: 2022-08-02

On-Brand Devices [Phase 4 Gel®]

• 00696588005621: Sample Phase 4 Gel® Splint - Non Sterile (1 each)
• 00696588003627: Phase 4 Gel® Splint - Non Sterile (10/case)