InterCollagen Guide

GUDID 00852072007520

SIGMAGRAFT, INC.

Collagen dental regeneration membrane

• Primary Device ID: 00852072007520
• NIH Device Record Key: 774f2da4-da36-4f51-aed9-3914f8690c58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InterCollagen Guide
• Version Model Number: ICG1520
• Company DUNS: 078893672
• Company Name: SIGMAGRAFT, INC.
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• 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	00852072007520 [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: 2023-09-29
• Device Publish Date: 2023-09-21

On-Brand Devices [InterCollagen Guide]

• 00852072007551: ICG3040
• 00852072007544: ICG2525
• 00852072007537: ICG2030
• 00852072007520: ICG1520