Disposable Non-electric Biopsy Forceps

GUDID 16970057574049

Jiangsu Vedkang Medical Science and Technology Co.,Ltd.

Flexible endoscopic biopsy forceps, single-use

• Primary Device ID: 16970057574049
• NIH Device Record Key: 1d42cc7a-9294-42c7-a84a-4983918b5ef1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Non-electric Biopsy Forceps
• Version Model Number: VDK-FB-23-230-O-P-A1
• Company DUNS: 544430136
• Company Name: Jiangsu Vedkang Medical Science and Technology Co.,Ltd.
• 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: 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	06970057574042 [Primary]
GS1	16970057574049 [Package]; Contains: 06970057574042; Package: box [10 Units]; In Commercial Distribution
GS1	56970057574047 [Package]; Package: carton [10 Units]; In Commercial Distribution

FDA Product Code

• FCL: Forceps, Biopsy, Non-Electric

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: 2024-08-26
• Device Publish Date: 2024-08-17

On-Brand Devices [Disposable Non-electric Biopsy Forceps]

• 16970057574179: VDK-FB-23-230-W-P-A1
• 16970057574049: VDK-FB-23-230-O-P-A1
• 16941513202486: VDK-FB-30-230-W-P1-A1