Disposable Biopsy Forceps

GUDID 06970900853133

Yangzhou Fartley Medical Instrument Technology Co., Ltd

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• Primary Device ID: 06970900853133
• NIH Device Record Key: eaa1fd8b-f0c8-46c3-ac84-dff7c264ba7a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Biopsy Forceps
• Version Model Number: FTL-BF-23-230-W-O-R
• Company DUNS: 544375774
• Company Name: Yangzhou Fartley Medical Instrument 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: false
• 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	06970900853133 [Primary]

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: 2023-10-26
• Device Publish Date: 2023-10-18

On-Brand Devices [Disposable Biopsy Forceps]

• 06970900857407: FTL-BF-30-230-W-O-R
• 06970900853133: FTL-BF-23-230-W-O-R
• 06970900853126: FTL-BF-23-230-W-O-A