Bard

GUDID 36945630135805

Sterilance Medical (Suzhou) Inc.

Scalpel, single-use

• Primary Device ID: 36945630135805
• NIH Device Record Key: c0ea72ec-455e-4ecd-be8e-2afc1571ade6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard
• Version Model Number: RM0752754
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 1500
• 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	06945630135804 [Primary]
GS1	36945630135805 [Unit of Use]

FDA Product Code

• GDX: Scalpel, One-Piece

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-31
• Device Publish Date: 2025-03-21

On-Brand Devices [Bard]

• 06945630114083: 22-0311B
• 36945630135805: RM0752754