GlasSpan Dental Fiber

GUDID D844G112

GLASSPAN INC

Dental reinforcing fibre Dental reinforcing fibre

• Primary Device ID: D844G112
• NIH Device Record Key: 64d25878-a9e6-4871-a6b4-1326afdf727d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GlasSpan Dental Fiber
• Version Model Number: Small Rope
• Company DUNS: 838967594
• Company Name: GLASSPAN INC
• Device Count: 3
• 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: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 610-363-7573
• Email: JAlan@glasspan.com
• Phone: 610-363-7573
• Email: JAlan@glasspan.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D844G101 [Unit of Use]
HIBCC	D844G112 [Primary]

FDA Product Code

• EBI: Resin, Denture, Relining, Repairing, Rebasing

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-21

On-Brand Devices [GlasSpan Dental Fiber]

• D844G415: Tape
• D844G314: Large Rope
• D844G213: Medium Rope
• D844G112: Small Rope