AccessGUDID - DEVICE: Reveal HD Bulk (30810111542631)

GUDID

Device Identifier (DI) Information

Brand Name: Reveal HD Bulk
Version or Model: H-9334B1
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: H-9334B1
Company Name: BISCO INC.

Primary DI Number: 30810111542631
Issuing Agency: GS1
Commercial Distribution End Date: January 26, 2023
Device Count: 50
Labeler D-U-N-S® Number*: 053529939 *Terms of Use
Previous DI: D757H9334B10

Device Description: Reveal HD Bulk B1 50ct Unit Dose (0.25g ea)

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 [?]
K171147	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 20 and 25 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b0644b0e-baea-4bb4-ba7e-dd0deded8ae6
Public Version Date: January 27, 2023
Public Version Number: 2
DI Record Publish Date: November 17, 2022