Personal Touch

GUDID 00860014873256

Bottom Line Solutions LLC

Surgical/examination garment kit

• Primary Device ID: 00860014873256
• NIH Device Record Key: f5598e7d-c04b-4fbb-9505-e34dacace602
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Personal Touch
• Version Model Number: PTGN303
• Company DUNS: 144893106
• Company Name: Bottom Line Solutions LLC
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Manufacturing Date: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860014873249 [Primary]
GS1	00860014873256 [Package]; Contains: 00860014873249; Package: [600 Units]; In Commercial Distribution
GS1	10860014873246 [Unit of Use]

FDA Product Code

• LZA: Polymer Patient Examination Glove

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: 2026-01-21
• Device Publish Date: 2026-01-13

On-Brand Devices [Personal Touch]

• 00860014873270: PTGN304
• 00860014873256: PTGN303
• 00860014873232: PTGN302
• 00860014873218: PTGN301