ManaMed Inc PTECH01

GUDID 00810113682488

The PrevenTech is intended to be an easy to use sequential compression system, prescribed by a physician, for use in the home or clinical setting to help prevent the onset of DVT in patients by stimulating blood flow in the extremities (stimulating muscle contractions). This device can be used to: Aid in the prevention of DVT Enhance blood circulation Diminish post-operative pain and swelling Reduce wound healing time Aid in the treatment and healing of: stasis dermatitis, venous stasis ulcers, arterial and diabetic leg ulcers, chronic venous insufficiency and reduction of edema in the lower limbs.

MANAMED INC

Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use Multi-chamber venous compression system garment, single-use
Primary Device ID00810113682488
NIH Device Record Keyff98854a-1dd7-46db-b3b3-8c5a7ff1b0f0
Commercial Distribution StatusIn Commercial Distribution
Brand NameManaMed Inc
Version Model NumberPrevenTech
Catalog NumberPTECH01
Company DUNS084042331
Company NameMANAMED 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 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

Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net
Phone888-508-0712
Emailsupport@manamed.net

Operating and Storage Conditions

Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius
Handling Environment TemperatureBetween 10 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100810113682488 [Primary]

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 Date2022-08-30
Device Publish Date2022-08-22

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