Bard

GUDID 06945630114083

Sterilance Medical (Suzhou) Inc.

Scalpel, single-use

• Primary Device ID: 06945630114083
• NIH Device Record Key: eaeef3ec-8e72-4a43-a629-752702a2a343
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard
• Version Model Number: 22-0311B
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 30
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945630114083 [Unit of Use]
GS1	16945630114080 [Primary]

FDA Product Code

• GDX: Scalpel, One-Piece

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: 2025-03-10
• Device Publish Date: 2025-02-28

On-Brand Devices [Bard]

• 06945630114083: 22-0311B
• 36945630135805: RM0752754