AeroDVx™, Arm Small DV-AS

GUDID 00856525007839

The AeroDVx ™ Arm System is comprised of a gradient compression sleeve, electronic intermittent pneumatic pump intermittent pneumatic compression for compression therapy or DVT Prophylaxis. The AeroDVx™ Arm gradient compression sleeve is a non-sterile single patient use medical device. The AeroDVx™ Arm Gradient Compression Sleeve contains a single bladder with a built-in gradient profile and inelastic straps to affix it to the patient’s Arm, and attached and unattached liner. An inflation source is attached to the inflation valve on the sleeve. There is an inflation sources provided: a portable, battery-operated intermittent pneumatic pump, to provide intermittent pneumatic compression. The system is intended for hospital and outpatient use.

SUN SCIENTIFIC, INC.

Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump Intermittent venous compression system pump
Primary Device ID00856525007839
NIH Device Record Keya6e3a63a-0f8f-4647-b55d-614c961dd347
Commercial Distribution Discontinuation2030-10-31
Commercial Distribution StatusIn Commercial Distribution
Brand NameAeroDVx™, Arm Small
Version Model NumberSmall Arm
Catalog NumberDV-AS
Company DUNS609397224
Company NameSUN SCIENTIFIC, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100856525007839 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JOWSleeve, Limb, Compressible

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-08
Device Publish Date2023-02-28

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