AccessGUDID - DEVICE: Extraction cannula (04260170881434)

GUDID

Device Identifier (DI) Information

Brand Name: Extraction cannula
Version or Model: Extraction cannula, 300 mm
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 665010-5
Company Name: Human Med AG

Primary DI Number: 04260170881434
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 332719157 *Terms of Use

Device Description: Extraction cannula, 300 mm, for fat extraction from container into syringe.

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?
56639	Collection syringe adaptor, single-use	A small sterile device designed be placed over the top of a syringe to encase the tip of the syringe as means to modify the shape and the size of the syringe tip. It is typically made of polymer material and its shape and size mimics that of the appropriately-matched syringe barrel (i.e., 60 cc, 30 cc, 10 cc versions of a Toomey style syringe). It is typically used for the transfer of human tissue or other substances from one container to another during plastic and reconstructive surgery, cosmetic surgery, or general surgery procedures. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
QKL	Lipoaspirate Washing System For Aesthetic Body Contouring

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: 61a79017-1102-4b7b-bf96-63bfc9cc718e
Public Version Date: August 07, 2025
Public Version Number: 1
DI Record Publish Date: July 30, 2025