Hydrophobic Filter-set 300005

GUDID 04260170881564

Hydrophobic Filter-set for Q-graft control overflow protection

Human Med AG

Stromal vascular fraction recovery set
Primary Device ID04260170881564
NIH Device Record Key12062147-c3aa-4bde-a673-7df41224dcf2
Commercial Distribution StatusIn Commercial Distribution
Brand NameHydrophobic Filter-set
Version Model NumberHydrophobic Filter-set for Q-graft control
Catalog Number300005
Company DUNS332719157
Company NameHuman Med AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com
Phone+49385395700
Emailinfo@humanmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104260170881564 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QPBSystem, Suction, Lipoplasty For Removal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-08-07
Device Publish Date2025-07-30

On-Brand Devices [Hydrophobic Filter-set]

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