Dura Separator, Standard, Reusable 800-712

GUDID 00810607000545

Dura Separator, Standard, Reusable 6.0mm #2

ACRA-CUT INC

Neurosurgical probe Neurosurgical probe

• Primary Device ID: 00810607000545
• NIH Device Record Key: c746083d-052a-4345-aff0-ec3dd193c804
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dura Separator, Standard, Reusable
• Version Model Number: 800-712
• Catalog Number: 800-712
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810607000545 [Primary]

FDA Product Code

• HAO: Instrument, Surgical, Non-Powered

Sterilization

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

[00810607000545]

Moist Heat or Steam Sterilization

[00810607000545]

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 [Dura Separator, Standard, Reusable]

• 00810607000569: Dura Separator, Standard, Reusable Set Consisting Of One Each #0 Cat#800-710 ID#00810607000521
• 00810607000552: Dura Separator, Standard, Reusable 8.0mm #3 (Similar to Penfield#3)
• 00810607000545: Dura Separator, Standard, Reusable 6.0mm #2
• 00810607000538: Dura Separator, Standard, Reusable 4.0mm #1
• 00810607000521: Dura Separator, Standard, Reusable 2.5mm #0