ACRA-CUT 210-221

GUDID 00810607002211

Disposable Cranial Perforator

ACRA-CUT INC

Automatic cranial perforator, single-use Automatic cranial perforator, single-use

• Primary Device ID: 00810607002211
• NIH Device Record Key: 57c8e039-f9ab-4d4b-820a-a0b16243fafa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACRA-CUT
• Version Model Number: 14/11mm CDM
• Catalog Number: 210-221
• Company DUNS: 612611459
• Company Name: ACRA-CUT INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	00810607002211 [Primary]

FDA Product Code

• HBF: Drills, Burrs, Trephines & Accessories (Compound, Powered)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-11-22
• Device Publish Date: 2016-09-23

On-Brand Devices [ACRA-CUT]

• 00810607002839: Disposable Cranial Perforator
• 00810607002754: Disposable Cranial Perforator
• 00810607002716: Disposable Cranial Perforator
• 00810607002556: Disposable Cranial Perforator
• 00810607002532: Disposable Cranial Perforator
• 00810607002518: Disposable Cranial Perforators
• 00810607002433: Disposable Cranial Perforator
• 00810607002419: Disposable Cranial Perforator
• 00810607002310: Disposable Cranial Perforator
• 00810607002211: Disposable Cranial Perforator
• 00810607002006: Disposable Cranial Perforator