INTERNA® UNIVERSAL IMPLANT ANALOG

GUDID 08435389804253

BIOTECHNOLOGY INSTITUTE SL

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 08435389804253
• NIH Device Record Key: 201ba007-13e9-408f-ab50-497a841ba217
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTERNA® UNIVERSAL IMPLANT ANALOG
• Version Model Number: INRLIU
• Company DUNS: 461665312
• Company Name: BIOTECHNOLOGY INSTITUTE SL
• 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: true
• Lot Batch: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08435389804253 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2022-11-17
• Device Publish Date: 2022-11-09

On-Brand Devices [INTERNA® UNIVERSAL IMPLANT ANALOG]

• 08435389804253: INRLIU
• 08435389826101: INRLIU