Biopsy kit

GUDID 08058964726018

G21 SRL

Vertebral bone biopsy procedure kit, single-use

• Primary Device ID: 08058964726018
• NIH Device Record Key: 0f76b75a-9ca2-48b7-913a-8a6708e3c9c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biopsy kit
• Version Model Number: VV 11 190 8
• Company DUNS: 431529195
• Company Name: G21 SRL
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	08058964726018 [Primary]

FDA Product Code

• MDM: Instrument, Manual, Surgical, General Use

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: 2024-10-22
• Device Publish Date: 2024-10-14

On-Brand Devices [Biopsy kit]

• 08058964726650: VV 10 190 8
• 08058964726018: VV 11 190 8
• 08058964725455: VV 13 190 8