Disposable Non-electric Biopsy Forceps

GUDID 16941513210979

Jiangsu Vedkang Medical Science and Technology Co.,Ltd.

Flexible endoscopic biopsy forceps, single-use

• Primary Device ID: 16941513210979
• NIH Device Record Key: 282507e3-a88f-4051-972e-dc6f53eeca09
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Non-electric Biopsy Forceps
• Version Model Number: VDK-FB-18-70-O-P-B1
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06941513210972 [Primary]
GS1	16941513210979 [Package]; Contains: 06941513210972; Package: BOX [10 Units]; In Commercial Distribution
GS1	56941513210977 [Package]; Contains: 06941513210972; Package: CASE [100 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: 2025-03-06
• Device Publish Date: 2025-02-26

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
• 16941513210979: VDK-FB-18-70-O-P-B1
• 16970057574483: VDK-FB-23-230-W-P1-A1