AccessGUDID - DEVICE: Liposat power infiltration pump (04260277173883)

GUDID

Device Identifier (DI) Information

Brand Name: Liposat power infiltration pump
Version or Model: 00002274
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Möller Medical GmbH

Primary DI Number: 04260277173883
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 320405061 *Terms of Use

Device Description: The "Liposat power" tumescence pump serves to guide a sodium chloride solution into human tissue in a sterile manner through a tube system using insertion needles. The "Liposat power" tumescence pump should be used only with the tube set from Möller Medical, "Liposat tube set for tumescence infiltration" (REF: 00002251).

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):	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?
36894	Liposuction system	An assembly of devices designed specifically to aspirate subcutaneous fat from the body by means of suction during a liposuction/lipectomy procedure. The system consists of an electrically-powered suction pump, typically with collection containers, tubing, and microbial/hydrophobic filters, and includes patient contact devices (e.g., handpiece/tip, cannula). The pump generates negative pressure for aspiration of fat through the patient contact device, which is inserted subcutaneously into the fat layer, and into the collection containers.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
QPB	System, Suction, Lipoplasty For Removal

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K053451	000

Device Exempt from Premarket Submission: No 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: 5ac12de1-4548-4f2d-9792-34cf4e374ad2
Public Version Date: March 30, 2022
Public Version Number: 5
DI Record Publish Date: September 24, 2016