AccessGUDID - DEVICE: Compspan™ Composite Luting Cement (D0026551001)

GUDID

Device Identifier (DI) Information

Brand Name: Compspan™ Composite Luting Cement
Version or Model: 655100
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 655100
Company Name: DENTSPLY INTERNATIONAL INC.

Primary DI Number: D0026551001
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 083235549 *Terms of Use

Device Description: Compspan™ Composite Luting Cement Complete Package

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:	Yes
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
EBH	MATERIAL, IMPRESSION TRAY, RESIN

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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
Special Storage Condition, Specify: Refrigeration extends shelf life. Shelf life is 12 months when stored at 75° F (24° C) or below.

Clinically Relevant Size

[?]

Size Type Text
Weight: 5 Gram
Device Size Text, specify: 1 base paste, 1 catalyst paste, 1 self-cure bonding agent base liquid, 1 self-cure bonding agent catalyst liquid, 1 bottle tooth conditioner gel, and accessories

Device Record Status

Public Device Record Key: fe49f016-fc01-4a83-b4eb-5c487965b6f8
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: September 21, 2016