Alton

GUDID 06970671381279

Alton (Shanghai) Medical Instruments Co., Ltd.

Flexible endoscopic biopsy forceps, single-use

• Primary Device ID: 06970671381279
• NIH Device Record Key: 79b898b2-f1a7-4c81-866a-38f423e7ef96
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alton
• Version Model Number: AF-D2423BWC
• Company DUNS: 527128502
• Company Name: Alton (Shanghai) Medical Instruments 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970671381279 [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: 2025-08-04
• Device Publish Date: 2025-07-25

On-Brand Devices [Alton]

• 06970671381903: AF-D2421GJ
• 06970671381873: AF-D1816GJ
• 06970671381408: AF-D2421BUC
• 06970671381279: AF-D2423BWC
• 06970671381255: AF-D2418BWC
• 06970671381132: AF-D2423BTC
• 06970671381118: AF-D2418BTC
• 06970671381095: AF-D1816BTC
• 06970671381088: AF-D1812BTC
• 06970671382023: AF-D2416GH
• 06970671382016: AF-D1816GH
• 06970671382009: AF-D1812GH
• 06970671381996: AF-D1810GH
• 06970671381880: AF-D2416GJ
• 06970671381866: AF-D1812GJ
• 06970671381811: AF-D2416GI
• 06970671381385: AF-D2416BUC
• 06970671381361: AF-D1812BUC