AccessGUDID - DEVICE: MIXPAC T-Mixer Blue/Orange Mixing Tips (00723896011119)

GUDID

Device Identifier (DI) Information

Brand Name: MIXPAC T-Mixer Blue/Orange Mixing Tips
Version or Model: 7075294
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 70-75294
Company Name: PRACTICON, INC.

Primary DI Number: 00723896011119
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 50
Labeler D-U-N-S® Number*: 119193803 *Terms of Use

Device Description: Decrease waste and reduce your overall cost with MIXPAC T-Mixer HP Mixing Tips! New technology provides a high mixing quality achieving more homogenous results. 100% compatible with original MIXPAC products. Tips available with color-trademarked domes consistent with the domes on standard MIXPAC mixing tips. Fits 4:1 or 10:1 cartridges.

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?
58399	Dental material mixing nozzle	A device designed for mixing inactive compounds during a dental procedure to produce a functional dental restorative/impression material which may be applied directly to the oral cavity/teeth of the patient or used for some other dental application. It is nozzle-shaped and has an integral mixing mechanism (e.g., spiralled channels). It is attached to the end of a cartridge consisting of two tubes so that the compounds are mixed as they are expressed simultaneously from the tubes through the nozzle. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EID	Syringe, Restorative And Impression Material

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: 55535eca-4b75-42d0-a54a-c79ee7d3ae93
Public Version Date: February 03, 2023
Public Version Number: 2
DI Record Publish Date: July 30, 2018