AccessGUDID - DEVICE: SprintRay Nightguard Flex 2 - Ocean Blue

GUDID

Device Identifier (DI) Information

Brand Name: SprintRay Nightguard Flex 2 - Ocean Blue - 1 Kg
Version or Model: SRI-0202146
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Sprintray, Inc.

Primary DI Number: 00850039704635
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 063005260 *Terms of Use

Device Description: SprintRay NightGuard Flex 2 is indicated for the fabrication of dental appliances such as mouthguards and nightguards.

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?
16730	Dental appliance fabrication material, resin	A resin intended to be used in the dental laboratory to manufacture a patient-worn dental prosthesis or appliance (e.g., denture base, occlusal splint/night guard), that either: 1) polymerizes under heat (heat-cured), light (light-cured), and/or after a period of time (self-cured); or 2) can be shaped by a dental mill [e.g., based on computer-aided design/computer-aided manufacturing (CAD/CAM) technology]. It may in addition be intended to fabricate non-patient-worn devices (e.g., drilling templates using 3-D printing). After application, this material cannot be refabricated.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KMY	Positioner, Tooth, Preformed

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: Store NightGuard Flex 2 at 15-25oC (60-77oF) and avoid direct sunlight.
Special Storage Condition, Specify: Keep the bottle closed and/or the tank lid securely attached when not in use.
Special Storage Condition, Specify: Before disposal, completely polymerize.

Clinically Relevant Size

[?]

Size Type Text
Weight: 1 Kilogram

Device Record Status

Public Device Record Key: 69b2c90a-131b-4ae7-a180-4f3f5f3c0e7a
Public Version Date: April 01, 2024
Public Version Number: 1
DI Record Publish Date: March 22, 2024