SYMBIOS® 59-8000

GUDID 07392532233357

SinusSet

Dentsply Implants Manufacturing GmbH

Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: 07392532233357
• NIH Device Record Key: 20fb105a-8969-4944-9c7c-8203846f2ba7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SYMBIOS®
• Version Model Number: 59-8000
• Catalog Number: 59-8000
• Company DUNS: 344038836
• Company Name: Dentsply Implants Manufacturing GmbH
• 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: 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	07392532233357 [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: 2022-07-25
• Device Publish Date: 2022-07-15

On-Brand Devices [SYMBIOS®]

• EFRIOSTRNRM25301: OsteoShield® Titanium-Reinforced Non-Resorbable Membrane (25x30mm)
• EFRIOSTRNRM12201: OsteoShield® Titanium-Reinforced Non-Resorbable Membrane (12x20mm)
• EFRIOSNRM25301: OsteoShield® PTFE Non-Resorbable Membrane (25x30mm)
• EFRIOSNRM12241: OsteoShield® PTFE Non-Resorbable Membrane (12x24mm)
• EFRIOSCRM30401: OsteoShield® Collagen Resorbable Membrane (30x40mm)
• EFRIOSCRM20301: OsteoShield® Collagen Resorbable Membrane (20x30mm)
• EFRIOSCRM15201: OsteoShield® Collagen Resorbable Membrane (15x20mm)
• EFRI9700003042: OSTEOGRAF/N-700 (4x3.0g)
• EFRI9700001042: OSTEOGRAF/N-700 (4x1.0g)
• EFRI9400003042: OSTEOGRAF/LD-300 (4x3.0g)
• EFRI9400001042: OSTEOGRAF/LD-300 (4x1.0g)
• EFRI9400000542: OSTEOGRAF /LD-300 (4x0.5g)
• EFRI9300003042: OSTEOGRAF/N-300 (4x3.0g)
• EFRI9300001042: OSTEOGRAF/N-300 (4x1.0g)
• EFRI9200001042: OSTEOGRAF/D-300 (4x1.0g)
• EFRI9000003042: OSTEOGRAF/D-700 (4x3.0g)
• EFRI9000001042: OSTEOGRAF/D-700 (4x1.0g)
• D716OSTRNRM25301: OsteoShield® Titanium-Reinforced Non-Resorbable Membrane (25x30mm)
• D716OSTRNRM12201: OsteoShield® Titanium-Reinforced Non-Resorbable Membrane (12x20mm)
• D716OSNRM25301: OsteoShield® PTFE Non-Resorbable Membrane (25x30mm)
• D716OSNRM12241: OsteoShield® PTFE Non-Resorbable Membrane (12x24mm)
• EFRI325974022: Symbios BoneShield rectangular 33x25 mm
• EFRI325974012: Symbios BoneShield triangular 21x17 mm
• EFRI325974002: Symbios BoneShield oval 20x15 mm
• 07392532233357: SinusSet
• 07392532239052: Symbios BoneShield rectangular 33x25 mm
• 07392532239045: Symbios BoneShield triangular 21x17 mm