quasar® lt med cos30003va19

GUDID 04050588000516

h/p/cosmos sports & medical gmbh

Cardiopulmonary stress test treadmill

• Primary Device ID: 04050588000516
• NIH Device Record Key: bb6b9f0a-8fb0-4d60-af98-2d25c4894e92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: quasar® lt med
• Version Model Number: cos30003va19
• Catalog Number: cos30003va19
• Company DUNS: 341362614
• Company Name: h/p/cosmos sports & medical 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04050588000516 [Primary]

FDA Product Code

• IOL: Treadmill, Powered

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: 2020-05-19
• Device Publish Date: 2020-01-07

Devices Manufactured by h/p/cosmos sports & medical gmbh

• 04050588000059 - stratos® lt med: 2020-05-19
• 04050588000066 - stratos® med: 2020-05-19
• 04050588000073 - mercury® lt med: 2020-05-19
• 04050588000080 - mercury® med: 2020-05-19
• 04050588000295 - locomotion® 150/50 E med: 2020-05-19
• 04050588000493 - stellar® lt med: 2020-05-19
• 04050588000509 - stellar® med: 2020-05-19
• 04050588000516 - quasar® lt med: 2020-05-19
• 04050588000516 - quasar® lt med: 2020-05-19