AccessGUDID - DEVICE: TPH Spectra ST flow (D0106425161)

GUDID

Device Identifier (DI) Information

Brand Name: TPH Spectra ST flow
Version or Model: 642516
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 642516
Company Name: Dentsply De Trey GmbH

Primary DI Number: D0106425161
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 16
Labeler D-U-N-S® Number*: 315471722 *Terms of Use

Device Description: TPH Spectra ST flow Compula Refill BW is a visible light cured, radiopaque composite resin restorative material with flow characteristics that make it ideal for use in anterior and posterior teeth.

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:	Yes
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
EBF	Material, tooth shade, resin

FDA Premarket Submission

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

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
Special Storage Condition, Specify: Do not freeze.
Storage Environment Temperature: between 2 and 28 Degrees Celsius
Special Storage Condition, Specify: Keep out of direct sunlight and protect from moisture.
Special Storage Condition, Specify: Store in a well-ventilated place.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b316d9ce-ec96-4d15-b0e2-d31b5a976286
Public Version Date: March 05, 2024
Public Version Number: 1
DI Record Publish Date: February 26, 2024