Fischer

GUDID M730MD20

Fischer Model MD-2 Galvanic Unit

A. R. HINKEL CO., INC.

Hyperhidrosis iontophoresis system

• Primary Device ID: M730MD20
• NIH Device Record Key: 7e4f4722-b78e-4b39-a4a6-3521c5d345c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fischer
• Version Model Number: MD-2 Galvanic Unit
• Company DUNS: 077962363
• Company Name: A. R. HINKEL CO., INC.
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8005253467
• Email: desk@rafischer.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M730MD20 [Primary]

FDA Product Code

• EGJ: Device, Iontophoresis, Other Uses

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-06-07
• Device Publish Date: 2014-09-16

On-Brand Devices [Fischer]

• M730MD20: Fischer Model MD-2 Galvanic Unit
• M730MD1A0: Fischer Model MD-1a Galvanic unit