AccessGUDID - DEVICE: MAXCUT DIAMOND BURS (6/pk) MED 850-023 (D778100850231)

GUDID

Device Identifier (DI) Information

Brand Name: MAXCUT DIAMOND BURS (6/pk) MED 850-023
Version or Model: 100-850-23
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 100-850-23
Company Name: SCOTT'S DENTAL SUPPLY L.L.C.

Primary DI Number: D778100850231
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 6
Labeler D-U-N-S® Number*: 137217043 *Terms of Use

Device Description: MAXCUT DIAMOND BURS (6/pk) Shape: Round End Taper; Size (in 1/10mm): 023; Grit: Medium; For more information: https://www.scottsdental.com/burs/diamond-burs/round-end-taper-multi-use-diamond-burs-maxcut.html

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):	No
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?
16670	Diamond dental bur, reusable	A rotary cutting device made of high-grade steel with the working end coated with particles of diamond, and which is designed to fit into a dental handpiece that provides the rotation allowing the user to cut hard structures in the mouth, such as teeth or bone. It can also be used to cut hard metals, plastics, porcelains and similar materials intended for use in the fabrication of dental devices. It is available in various shapes (e.g., cylinder, disk, sphere, oval). This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EJL	BUR, DENTAL

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: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: a83813dc-3720-43d8-ab14-d10823ffc2b0
Public Version Date: October 14, 2020
Public Version Number: 1
DI Record Publish Date: October 06, 2020