Prestige Medical 23-S

GUDID 00786511787585

QUEEN SQUARE HAMMER-11.5 INCH-BULK

RASHMAN CORPORATION

Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable Percussion hammer, manual, reusable

• Primary Device ID: 00786511787585
• NIH Device Record Key: 0545b01d-4484-478a-9d8a-a393278a4bef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Prestige Medical
• Version Model Number: 23-S
• Catalog Number: 23-S
• Company DUNS: 078803608
• Company Name: RASHMAN CORPORATION
• 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: false
• Serial Number: false
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00786511787585 [Primary]

FDA Product Code

• GWZ: Percussor

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: 2020-10-16
• Device Publish Date: 2020-10-08

On-Brand Devices [Prestige Medical]

• 00786511242640: PREMIUM ANEROID BP-POR W/CASE-BX
• 00786511242633: PREMIUM ANEROID BP-POB W/CASE-BX
• 00786511787585: QUEEN SQUARE HAMMER-11.5 INCH-BULK