ADVAN

GUDID 26944875700031

Ningbo Advan Electrical Co., Ltd.

Skin staple remover, single-use

• Primary Device ID: 26944875700031
• NIH Device Record Key: 91277eb6-5ec5-41a2-9b19-bcc29a055dc8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ADVAN
• Version Model Number: C-W
• Company DUNS: 723061094
• Company Name: Ningbo Advan Electrical 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	26944875700031 [Primary]

FDA Product Code

• MDM: Instrument, Manual, Surgical, General Use

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: 2022-10-18
• Device Publish Date: 2022-10-10

On-Brand Devices [ADVAN]

• 26944875700031: C-W
• 26944875700024: F-W
• 26944875700017: F-R