AccessGUDID - DEVICE: Endo Bendable Tip (D746TIP20060201)

GUDID

Device Identifier (DI) Information

Brand Name: Endo Bendable Tip
Version or Model: TIP2006020
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: TIP2006020
Company Name: DENTSPLY SIRONA ORTHODONTICS INC.

Primary DI Number: D746TIP20060201
Issuing Agency: HIBCC
Commercial Distribution End Date: February 19, 2021
Device Count: 20
Labeler D-U-N-S® Number*: 116903307 *Terms of Use

Device Description: Endo Bendable Tip 20mm 200uM box 20

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":	Yes
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?
60340	Dental diode laser system	A mains electricity (AC-powered) device assembly in which input energy is used to excite a diode to emit a high-power therapeutic laser beam intended to cut, excise, vaporize, and coagulate oral tissues in various dental applications such as oral soft-tissue surgery, gingivectomy, to diminish inflammation, and for oral therapy and tooth whitening; it is not a dedicated tooth-bleaching acceleration unit. It includes a portable diode laser light source, flexible fibreoptic delivery cable, and controls/foot-switch; it may include a rechargeable battery.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEX	Powered laser surgical instrument

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: a7866050-5d31-42c6-9f65-446ebed62f23
Public Version Date: April 03, 2024
Public Version Number: 5
DI Record Publish Date: September 24, 2016