Hammer

GUDID 00786511000264

Buck Neurological Hammer

RASHMAN CORPORATION

Percussion hammer, manual, reusable

• Primary Device ID: 00786511000264
• NIH Device Record Key: 09827ca3-1cf6-461f-a674-2b0459fa51a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hammer
• Version Model Number: 26
• 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	00786511000264 [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: 2022-12-12
• Device Publish Date: 2022-12-02

On-Brand Devices [Hammer ]

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• 00786511000288: Economy Taylor Percussion Hammer
• 00786511000264: Buck Neurological Hammer
• 00786511000240: Babinski Telescoping Reflex Hammer
• 00786511870256: Taylor Percussion Hammer
• 00786511630256: Taylor Percussion Hammer
• 00786511620257: Taylor Percussion Hammer
• 00786511247973: Taylor Percussion Hammer
• 00786511247966: Taylor Percussion Hammer
• 00786511075149: Taylor Percussion Hammer
• 00786511075132: Taylor Percussion Hammer
• 00786511000257: Taylor Percussion Hammer