INTERNA® NARROW MULTI-IM® ABUTMENT 5 MM

GUDID 08435389814535

BIOTECHNOLOGY INSTITUTE SL

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08435389814535
• NIH Device Record Key: 23bed664-70bc-4b5a-8d83-fe8315a78eb3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTERNA® NARROW MULTI-IM® ABUTMENT 5 MM
• Version Model Number: INTMIPE50
• Company DUNS: 461665312
• Company Name: BIOTECHNOLOGY INSTITUTE SL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• 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	08435389814535 [Primary]

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-22
• Device Publish Date: 2025-04-14

Devices Manufactured by BIOTECHNOLOGY INSTITUTE SL

• 08435389814535 - INTERNA® NARROW MULTI-IM® ABUTMENT 5 MM: 2025-04-22
• 08435389814535 - INTERNA® NARROW MULTI-IM® ABUTMENT 5 MM: 2025-04-22
• 08435389819042 - INTERNA 3.0 MULTI-IM ABUTMENT 2 MM: 2025-04-22
• 08435389819059 - INTERNA 3.0 MULTI-IM ABUTMENT 2.5 MM: 2025-04-22
• 08435389819066 - INTERNA 3.0 MULTI-IM ABUTMENT 3 MM: 2025-04-22
• 08435389819073 - INTERNA 3.0 IMPLANT CA Ø3 L10: 2025-04-22
• 08435389819097 - INTERNA 3.0 IMPLANT CA Ø3 L8,5: 2025-04-22
• 08435389819141 - INTERNA 3.0 TITANIUM BIOABUTMENT Ø3,4 L:3 MM: 2025-04-22
• 08435389819158 - INTERNA 3.0 TITANIUM BIOABUTMENT Ø3,4 L:4 MM: 2025-04-22