AccessGUDID - DEVICE: Bifix Hybrid Abutment Cement (E22124121)

GUDID

Device Identifier (DI) Information

Brand Name: Bifix Hybrid Abutment Cement
Version or Model: 2412
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 2412
Company Name: VOCO GmbH

Primary DI Number: E22124121
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 316699578 *Terms of Use

Device Description: Bifix Hybrid Abutment Cement is a radiopaque, composite-based, dual-curing cementation system for the permanent cementation of abutment crowns and mesostructures made of metal, ceramics or polymers (composite or PMMA) on prefabricated adhesive/titanium bases (extraoral use), customized abutments made of titanium or zirconium dioxide or dental hard tissue (combination solutions). 10g QM syringe white HO

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35870	Dental composite resin	A non-sterile substance intended for professional use as a dental luting agent, liner, base, pulp-capping material, pit/fissure sealant, and/or direct dental restorative material, whereby the majority of the setting reaction is based on the self-, light-, or dual-cured polymerization of a dimethacrylate resin [e.g., polymethylmethacrylate (PMMA), polyurethane, or bisphenol-A-diglycidylether methacrylate (Bis-GMA)]; it includes some additional fillers/components (e.g., glass-based, quartz, or ceramic). It may be preloaded into a syringe, and dedicated disposable devices associated with application may be included. After application, this device cannot be reused.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EMA	Cement, Dental

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K220640	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 4 and 23 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f75d7d16-0d93-42b0-95d1-1a01ba476e9b
Public Version Date: September 06, 2022
Public Version Number: 1
DI Record Publish Date: August 29, 2022