Maptag

GUDID 06975854035222

Sanwei Taige (Suzhou) Medical Co., Ltd.

Penile vacuum device

• Primary Device ID: 06975854035222
• NIH Device Record Key: 55b6a7d8-df32-4d9e-b67b-cb6835d44eeb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maptag
• Version Model Number: MP-3522
• Company DUNS: 844723005
• Company Name: Sanwei Taige (Suzhou) Medical 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	06975854035222 [Primary]

FDA Product Code

• LKY: Device, External Penile Rigidity

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-22
• Device Publish Date: 2022-11-14

On-Brand Devices [Maptag]

• 06975854035215: MP-3521
• 06975854035222: MP-3522
• 06975854036489: MNM-6489
• 06975854035734: BMG-5734