RADII 5600202

GUDID 09336472031053

RADII PLUS LED LGT ALL REG

SDI LIMITED

Dental/surgical polymerization lamp

• Primary Device ID: 09336472031053
• NIH Device Record Key: 8f715f7c-a8e9-41d5-b0f5-3cfae1b2f7b7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RADII
• Version Model Number: 5600202
• Catalog Number: 5600202
• Company DUNS: 753221852
• Company Name: SDI LIMITED
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.
• Special Storage Condition, Specify: Between 0 and 0 *Temperature controlled not required. Dried area.

Device Identifiers

Device Issuing Agency	Device ID
GS1	09336472031053 [Primary]

FDA Product Code

• EBZ: ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION

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: 2025-01-16
• Device Publish Date: 2025-01-08

On-Brand Devices [RADII]

• DO3656002021: RADII PLUS LED LGT ALL REG
• DO3656001021: RADII-CAL LED LGT ALL REG
• 09336472031053: RADII PLUS LED LGT ALL REG
• 09336472006488: RADII-CAL LED LGT ALL REG