Mamo Collimator

GUDID 00850816007164

DIGIRAD CORPORATION

Multi-hole nuclear medicine system collimator, low-energy

• Primary Device ID: 00850816007164
• NIH Device Record Key: d87cfc45-f076-4465-8809-85f23f9ae030
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mamo Collimator
• Version Model Number: Mamo
• Company DUNS: 148548738
• Company Name: DIGIRAD CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Customer Support Contacts

• Phone: 8587261600
• Email: callcenter@digirad.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850816007164 [Primary]

FDA Product Code

• IYX: Camera, Scintillation (Gamma)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-12

Devices Manufactured by DIGIRAD CORPORATION

• 00850816007195 - Breast Imaging Accessory: 2019-03-11
• 00850816007027 - LEHR Collimator: 2018-03-29
• 00850816007034 - Cardius 2: 2018-03-29
• 00850816007041 - Cardius 2: 2018-03-29
• 00850816007058 - Cardius 2: 2018-03-29
• 00850816007065 - Cardius 2: 2018-03-29
• 00850816007072 - Cardius 3: 2018-03-29
• 00850816007089 - Cardius 3: 2018-03-29