MAPTAG

GUDID 06975904970015

MAPTAG (QINGDAO) MEDICAL TECHNOLOGY CO., LTD.

Penile vacuum device

• Primary Device ID: 06975904970015
• NIH Device Record Key: d5c2f6b0-4bef-471a-aac9-c60a79a78ca2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAPTAG
• Version Model Number: MP-3521
• Company DUNS: 847743165
• Company Name: MAPTAG (QINGDAO) 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: 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	06975904970015 [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: 2023-04-14
• Device Publish Date: 2023-04-06