AccessGUDID - DEVICE: Accelerator III 2mm x 26cm Small Handle Cannula (00081317021018)

GUDID

Device Identifier (DI) Information

Brand Name: Accelerator III 2mm x 26cm Small Handle Cannula
Version or Model: III226S
Commercial Distribution Status: In Commercial Distribution
Catalog Number: III226S
Company Name: MENTOR TEXAS L.P.

Primary DI Number: 00081317021018
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 167450993 *Terms of Use

Device Description: Accelerator III 2mm x 26cm Small Handle Cannula

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:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Liposuction system cannula, reusable	A rigid tube that is inserted percutaneously to sites of fat deposits, and that functions as part of a lipectomy suction system for the aspiration of the fat during liposuction/lipoplasty. The device may also be used to infiltrate the operative site with a solution during the procedure, which is then aspirated. It is typically made of high-grade stainless steel. This is a reusable device.

FDA Product Code

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Product Code	Product Code Name
MUU	System, suction, lipoplasty

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K981172	000

Device Exempt from Premarket Submission: No 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

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Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 7c000b72-0d92-433f-8a2b-39417d6f90f0
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: September 23, 2016