inspiro Body i1

GUDID 07640163050134

inspiro Body i1 20 x 0.3 g Compule

EDELWEISS DR ag

Custom-made dental composite resin kit

• Primary Device ID: 07640163050134
• NIH Device Record Key: f85b083a-defc-449c-adfb-c3c5e7e97535
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: inspiro Body i1
• Version Model Number: 3215
• Company DUNS: 486793370
• Company Name: EDELWEISS DR ag
• Device Count: 20
• 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: false
• 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	07640163050134 [Primary]
GS1	76401630503215 [Unit of Use]

FDA Product Code

• EBF: Material, Tooth Shade, Resin

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: 2016-10-19

On-Brand Devices [inspiro Body i1 ]

• 07640163050301: inspiro Body i1
• 07640163050134: inspiro Body i1 20 x 0.3 g Compule
• 07640163050127: inspiro Body i1 10 x 0.3 g Compule