ABUTMENT MINI ANGLED MORSE TAPER Ø4,8X3X 45° INDEX MAAM 4843I

GUDID 07899995278036

ABUTMENT MINI ANGLED MORSE TAPER Ø4,8X3X 45° INDEX

Sin Sistema de Implante Nacional S/A

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07899995278036
• NIH Device Record Key: 09aa5174-d340-4dfe-acff-79f6af2393ca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ABUTMENT MINI ANGLED MORSE TAPER Ø4,8X3X 45° INDEX
• Version Model Number: MAAM 4843I
• Catalog Number: MAAM 4843I
• Company DUNS: 904569092
• Company Name: Sin Sistema de Implante Nacional S/A
• 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: true
• 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	07899995278036 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231127

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: 2023-12-26
• Device Publish Date: 2023-12-18

Devices Manufactured by Sin Sistema de Implante Nacional S/A

• 07899995201171 - ANILHA PARA GUIA CIRURGICO Ø4.1MM: 2024-01-01 ANILHA PARA GUIA CIRURGICO Ø4.1MM
• 07899995201270 - DRIVER HANDPIECE IMP. TRYON GUIDED: 2024-01-01 DRIVER HANDPIECE IMP. TRYON GUIDED
• 07899995203120 - DRIVE ANGLED BONE GRAFT: 2024-01-01 DRIVE ANGLED BONE GRAFT
• 07899995203144 - DRIVER ORTHODONTIC: 2024-01-01 DRIVER ORTHODONTIC
• 07899995205049 - CHAVE DE CATRACA: 2024-01-01 CHAVE DE CATRACA
• 07899995206282 - DRIVER HANDPIECE IMP. CM: 2024-01-01 DRIVER HANDPIECE IMP. CM
• 07899995206299 - DRIVER HANDPIECE IMP. CM: 2024-01-01 DRIVER HANDPIECE IMP. CM
• 07899995207203 - DRIVER HANDPIECE IMP. 24MM: 2024-01-01 DRIVER HANDPIECE IMP. 24MM