Single Use Biopsy Forceps

GUDID 26970401813319

Zhe Jiang ChuangXiang Medical Technology Co., Ltd.

Flexible endoscopic biopsy forceps, single-use

• Primary Device ID: 26970401813319
• NIH Device Record Key: 1d4b4f3e-f872-4bd2-8a25-7fad278f4da1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Use Biopsy Forceps
• Version Model Number: MD-C-BF2423
• Company DUNS: 544434963
• Company Name: Zhe Jiang ChuangXiang Medical 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	06970401810284 [Primary]
GS1	16970401813305 [Package]; Contains: 06970401810284; Package: Box [10 Units]; In Commercial Distribution
GS1	26970401813319 [Package]; Contains: 16970401813305; Package: Case [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: 2018-10-29
• Device Publish Date: 2018-09-27

On-Brand Devices [Single Use Biopsy Forceps]

• 26970401813364: MD-C-BF1823
• 26970401813333: MD-C-BF1818
• 26970401813319: MD-C-BF2423
• 16970401813671: MD-B-BF2423
• 26970401813517: MD-A-BF2423
• 26970401813401: MD-A-BF2416
• 26970401813944: MD-A-BF2418
• 26970401813975: MD-C-BF2403
• 26970401814248: MD-B-BF2418