AccessGUDID - DEVICE: Total-Comfort Clear Soft Tip Aspirators White Tubing (00723896009895)

GUDID

Device Identifier (DI) Information

Brand Name: Total-Comfort Clear Soft Tip Aspirators White Tubing
Version or Model: K2900-BTS155TC
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 70-24911 WHI
Company Name: PRACTICON, INC.

Primary DI Number: 00723896009895
Issuing Agency: GS1
Commercial Distribution End Date: July 20, 2018
Device Count: 100
Labeler D-U-N-S® Number*: 119193803 *Terms of Use

Device Description: ard plastic tip saliva ejectors are just that-hard! They pinch lingual surfaces, jab the mandible and aspirate tender tissue. Here is a truly comfortable solution-so comfortable, it's patented! Total-Comfort Soft Tip Aspirators feature cushioned, flexible, patient-friendly tips. Tested and proven to be gentle on soft tissue and bone while reducing soft tissue aspiration. Elastic tips are securely bonded for safety. 100% non-latex. 6" long. 100 aspirators per bag with white or clear tubing.

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):	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?
37434	Dental suction system cannula, single-use	A semi-rigid or rigid hollow tubular component of a dental suction system designed to be inserted into the oral cavity for the aspiration and removal of blood, pus, saliva, debris, and water during a dental procedure. It is typically made of disposable plastic materials. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EHZ	Evacuator, Oral Cavity

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 483c8ad5-9c02-4721-b693-3a5a73fe8c36
Public Version Date: June 12, 2023
Public Version Number: 2
DI Record Publish Date: July 19, 2018