Viamed Surgical Blades

GUDID 36945630112394

Sterilance Medical (Suzhou) Inc.

Manual scalpel blade, single-use

• Primary Device ID: 36945630112394
• NIH Device Record Key: ec1a89a6-9b7f-442b-a4aa-7faafcf361d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Viamed Surgical Blades
• Version Model Number: 11#
• Company DUNS: 554434897
• Company Name: Sterilance Medical (Suzhou) Inc.
• Device Count: 100
• 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: 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	06945630112393 [Unit of Use]
GS1	16945630112390 [Primary]
GS1	36945630112394 [Package]; Contains: 16945630112390; Package: [5000 Units]; In Commercial Distribution

FDA Product Code

• GES: Blade, Scalpel

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: 2022-05-26
• Device Publish Date: 2022-05-18

On-Brand Devices [Viamed Surgical Blades]

• 36945630112462: 24#
• 36945630112455: 23#
• 36945630112448: 22#
• 36945630112431: 21#
• 36945630112424: 20#
• 36945630112417: 15#
• 36945630112400: 12#
• 36945630112394: 11#
• 36945630112387: 10#
• 36945630121662: 15C