Bone Pad Remover, Reusable 800-020L

GUDID 00810607000507

Left Hand Bone Pad Remover, Reusable

ACRA-CUT INC

Neurosurgical probe

• Primary Device ID: 00810607000507
• NIH Device Record Key: 0f6b5749-b56f-458b-a620-6d125e4d2bde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bone Pad Remover, Reusable
• Version Model Number: 800-020L
• Catalog Number: 800-020L
• Company DUNS: 612611459
• Company Name: ACRA-CUT INC
• 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: true
• 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

Customer Support Contacts

• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810607000507 [Primary]

FDA Product Code

• HAO: Instrument, Surgical, Non-Powered

Sterilization

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

[00810607000507]

Moist Heat or Steam Sterilization

[00810607000507]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-08-01

On-Brand Devices [Bone Pad Remover, Reusable]

• 00810607000514: Right Hand Bone Pad Remover, Reusable
• 00810607000507: Left Hand Bone Pad Remover, Reusable