AccessGUDID - DEVICE: Tatum EZ Out Periotome E Kit (00083208162220)

GUDID

Device Identifier (DI) Information

Brand Name: Tatum EZ Out Periotome E Kit
Version or Model: Tatum EZ Out Periotome E Kit
Commercial Distribution Status: In Commercial Distribution
Catalog Number: Tatum EZ Out Periotome E Kit
Company Name: Suncoast Dental, Inc

Primary DI Number: 00083208162220
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 078352849 *Terms of Use

Device Description: Tatum EZ Out Periotome E Kit - for Atraumatic extraction of roots and teeth - Inc box and 7 periotomes #1,#2, #3, #4, #5, #6, & #7, and a sharpening stone

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:	Yes
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?
45713	Periotome, reusable	A hand-held dental instrument intended to be used during tooth extraction/luxation to cut the periodontal ligament that binds the tooth to the surrounding marginal and alveolar bone (alveolar process), causing minimal mechanical trauma to the bone tissue. It is typically made of stainless steel and consists of a shaft that terminates in a single or double flat, sharpened blade that is straight, curved, or angled. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EMJ	Elevator, Surgical, 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: 83abb8a9-35b2-4cd1-bdde-4f8458f017a2
Public Version Date: August 07, 2024
Public Version Number: 1
DI Record Publish Date: July 30, 2024