SwissGraft X D-Line

GUDID 07610221010158

Geistlich Pharma AG

Dental bone matrix implant, animal-derived

• Primary Device ID: 07610221010158
• NIH Device Record Key: 74287c59-1b57-4746-af22-fc6778b4a5aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SwissGraft X D-Line
• Version Model Number: 502081
• Company DUNS: 480781728
• Company Name: Geistlich Pharma AG
• Device Count: 1
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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 Dimensions

• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram
• Weight: 0.3 Gram

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221010158 [Primary]

FDA Product Code

• NPM: Bone Grafting Material, Animal Source

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: 2025-08-11
• Device Publish Date: 2025-08-01

On-Brand Devices [SwissGraft X D-Line]

• 07610221015382: 502083
• 07610221015375: 502082
• 07610221010158: 502081
• 07610221010141: 502080