AccessGUDID - DEVICE: INVASIVE ACCESSORIES AND INSTRUMENTS (08059224002415)

GUDID

Device Identifier (DI) Information

Brand Name: INVASIVE ACCESSORIES AND INSTRUMENTS
Version or Model: Extractor Kit X TRI Matrix® P37
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 680M-P37
Company Name: RHEIN 83 SRL

Primary DI Number: 08059224002415
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 439240722 *Terms of Use

Device Description: BROKEN SCREW EXTRACTOR KIT is a system that allow to remove broken thread into a fixture when it is not cemented or damaged attempting to remove it in other way.

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?
16668	Carbide dental bur, reusable	A rotary cutting device made of high-grade steel, the working end of which is made from, or coated with, tungsten carbide, and which is designed to fit into a dental handpiece that provides the rotation allowing the user to cut hard structures in the mouth, e.g., teeth or bone. It can also be used to cut hard metals, plastics, porcelains and similar materials. 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
DZA	Drill, Dental, Intraoral

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: 8a76b2d6-7054-40d0-a5e1-45aeb683ee24
Public Version Date: March 15, 2024
Public Version Number: 1
DI Record Publish Date: March 07, 2024