GFS Procedure Kit la524dis-setst

GUDID 10810128461624

T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION

Arthroscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 10810128461624
• NIH Device Record Key: 55ee4517-f1e0-4bd3-84bf-6898652bdbe2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GFS Procedure Kit
• Version Model Number: 3910-800-000
• Catalog Number: la524dis-setst
• Company DUNS: 534123013
• Company Name: T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
• 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: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10810128461624 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-19
• Device Publish Date: 2026-01-11

Devices Manufactured by T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION

• 10810128461792 - GFS Hohmann Retractor: 2026-01-26
• 10810128461808 - GFS Glenoid Lever, Double Prong: 2026-01-26
• 10810128461815 - GFS Subscapularis Spreader: 2026-01-26
• 10810128461822 - GFS Glenoid Drill: 2026-01-26
• 10810128461839 - GFS Glenoid Guide: 2026-01-26
• 10810128461846 - GFS Small Probe: 2026-01-26
• 10810128461655 - GFS Switching Stick: 2026-01-23
• 10810128461662 - GFS Inline Coracoid Drill Guide: 2026-01-23