BIODAM SAMPLLABIOBLU01800501

GUDID 05060748682956

BIODAM Sample Blue Latex Dam - Medium 5" - 1pc

FOUR D RUBBER COMPANY LIMITED

Rubber dam, Hevea-latex

• Primary Device ID: 05060748682956
• NIH Device Record Key: 63e1b0d5-fa05-4e79-8bfa-81db33ff5967
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BIODAM
• Version Model Number: Medium
• Catalog Number: SAMPLLABIOBLU01800501
• Company DUNS: 221795755
• Company Name: FOUR D RUBBER COMPANY LIMITED
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com
• Phone: +4401773763134
• Email: Info@fourdrubber.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060748682956 [Primary]

FDA Product Code

• EIE: Dam, Rubber

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: 2024-12-26
• Device Publish Date: 2024-12-18

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