AccessGUDID - DEVICE: LG PT 15 - Lipogems Procedure Tray (08058773562890)

GUDID

Device Identifier (DI) Information

Brand Name: LG PT 15 - Lipogems Procedure Tray
Version or Model: LG PT 15
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: LIPOGEMS INTERNATIONAL SPA

Primary DI Number: 08058773562890
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 431081002 *Terms of Use

Device Description: LG PT 15 - Lipogems Procedure Tray (15 pieces - 3 cannulas)

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):	Yes
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?
56627	Autologous adipose tissue collection/washing set	A collection of sterile devices designed as a closed system for the harvesting and rapid treatment of autologous fat tissue for reinjection back into the patient from which it was taken for aesthetic body contouring. It typically consists of various chambers (e.g., a collection bag, waste material bag, and a cleaned tissue bag), flexible tubing, an intravenous (IV) spike for connection to the washing solutions, and a contiguous filter mesh which dialyses the fat graft. It is used in conjunction with appropriate IV solutions within the sterile field of intervention for plastic and reconstructive surgery and cosmetic surgery. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
QUB	Suction Lipoplasty System For Removal And Transfer

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
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: 48ebe1fb-0c73-4d54-a4c8-f893915b01e3
Public Version Date: March 28, 2023
Public Version Number: 1
DI Record Publish Date: March 20, 2023