Rebilda Post GT

GUDID E22119751

5 posts à ø 1.2 mm

VOCO GmbH

Root canal post, preformed

• Primary Device ID: E22119751
• NIH Device Record Key: f19e153b-b03a-4381-9a1a-f46dcaf94b58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rebilda Post GT
• Version Model Number: 1975
• Company DUNS: 316699578
• Company Name: VOCO GmbH
• Device Count: 5
• 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: false
• 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

Customer Support Contacts

• Phone: 999-999-9999
• Email: xxx@xx.xx

Operating and Storage Conditions

• Storage Environment Temperature: Between 4 Degrees Celsius and 23 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E2211975 [Unit of Use]
HIBCC	E22119751 [Primary]

FDA Product Code

• ELR: Post, Root Canal

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: 2017-11-24

On-Brand Devices [Rebilda Post GT]

• E22119761: 5 posts à ø 1.4 mm
• E22119751: 5 posts à ø 1.2 mm
• E22119741: 5 posts à ø 1.0 mm
• E22119731: 5 posts à ø 0.8 mm
• E22119721: set, 5 posts each (~ ø 0,8 mm, ~ ø 1,0 mm, ~ ø 1,2 mm, ~ ø 1,4 mm), Ceramic Bond, Bottle, 5