GAMMA FINDER® III

GUDID 04056702007973

W.O.M. World of Medicine GmbH

Hand-held-detector nuclear medicine system

• Primary Device ID: 04056702007973
• NIH Device Record Key: 0e6bda3f-2974-4476-b04e-38ebf8e19413
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GAMMA FINDER® III
• Version Model Number: GAMMA FINDER® III
• Company DUNS: 316305242
• Company Name: W.O.M. World of Medicine GmbH
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056702007973 [Primary]

FDA Product Code

• IZD: Probe, Uptake, Nuclear

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: 2019-04-05
• Device Publish Date: 2019-03-28

On-Brand Devices [GAMMA FINDER® III ]

• 04056702007973: GAMMA FINDER® III
• 04056702006600: GAMMA FINDER® III