SwissMembrane X D-Line

GUDID 07610221010219

Geistlich Pharma AG

Collagen dental regeneration membrane

• Primary Device ID: 07610221010219
• NIH Device Record Key: 31adf491-d5d3-4f7d-8a19-7fb95df06d00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SwissMembrane X D-Line
• Version Model Number: 502088
• 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

• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter
• Width: 30 Centimeter
• Height: 40 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221010219 [Primary]

FDA Product Code

• NPL: Barrier, Animal Source, Intraoral

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 [SwissMembrane X D-Line]

• 07610221015429: 502087
• 07610221010257: 502089
• 07610221010219: 502088