Acu-Scissors

GUDID 00814105021118

Acu-Scissors, Curved, Sterile, 5/Bx

ACUDERM, INC.

General-purpose surgical scissors, single-use

• Primary Device ID: 00814105021118
• NIH Device Record Key: 4682f59b-5370-4c37-b973-1db60fe0b76d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Acu-Scissors
• Version Model Number: SCC
• Company DUNS: 071426803
• Company Name: ACUDERM, INC.
• Device Count: 5
• 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: true
• 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	00814105021118 [Unit of Use]
GS1	10814105021115 [Primary]

FDA Product Code

• LRW: Scissors, General, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-30
• Device Publish Date: 2020-09-22

On-Brand Devices [Acu-Scissors]

• 00814105021118: Acu-Scissors, Curved, Sterile, 5/Bx
• 00814105021101: Acu-Scissors, Straight, Sterile, 5/Bx