NovoTHOR

GUDID 05060494130503

S2188 NovoTHOR

THOR PHOTOMEDICINE LIMITED

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• Primary Device ID: 05060494130503
• NIH Device Record Key: 438421a2-1ec5-4f83-a2e0-32beb3e34907
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NovoTHOR
• Version Model Number: 3.0
• Company DUNS: 856233908
• Company Name: THOR PHOTOMEDICINE LIMITED
• 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	05060494130503 [Primary]

FDA Product Code

• ILY: Lamp, Infrared, Therapeutic Heating

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: 2021-01-18
• Device Publish Date: 2021-01-08

Devices Manufactured by THOR PHOTOMEDICINE LIMITED

• 05060494130589 - LED Helmet: 2021-10-14 S2185 LED Helmet
• 05060494130596 - LED Helmet PRX: 2021-10-14 S2194 LED Helmet PRX
• 05060494130572 - LED Lollipop: 2021-10-11 S2197 LED Lollipop
• 05060494130541 - Lollipop Probe: 2021-05-25 S2197 Lollipop Probe
• 05060494130558 - 810nm 16W Cluster PRX100 (80x200mW): 2021-05-25 S2202 810nm 16W Cluster PRX100 (80x200mW)
• 05060494130565 - PRX Lollipop Probe: 2021-05-25 S2196 PRX Lollipop Probe
• 05060494130503 - NovoTHOR: 2021-01-18S2188 NovoTHOR
• 05060494130503 - NovoTHOR: 2021-01-18 S2188 NovoTHOR
• 05060494130510 - NovoTHOR XL: 2021-01-18 S2190 NovoTHOR XL