AirSculpt Air Hose (IN)

GUDID 00850000712461

Millennium Medical Technologies, Inc.

Liposuction system
Primary Device ID00850000712461
NIH Device Record Keyb47df6cc-3a6f-4865-a94e-2d4495a32d7b
Commercial Distribution StatusIn Commercial Distribution
Brand NameAirSculpt Air Hose (IN)
Version Model NumberTD-10010
Company DUNS968286021
Company NameMillennium Medical Technologies, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100850000712461 [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 Date2025-06-11
Device Publish Date2025-06-03

Devices Manufactured by Millennium Medical Technologies, Inc.

00850000712201 - AirSculpt Console2025-06-12
00850000712379 - AirSculpt Handpiece2025-06-12
00850000712430 - AirSculpt Triple-Port Tubing2025-06-12
00850000712331 - AirSculpt System2025-06-11
00850000712461 - AirSculpt Air Hose (IN)2025-06-11
00850000712461 - AirSculpt Air Hose (IN)2025-06-11
00850000712423 - Acquicell Pro2025-05-02
00850000712096 - Infiltration Large Bore Tubing2023-08-15
00850000712119 - Disposable Fat Extraction cannula 3.4dis X 20cm2023-08-15

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.