FDA UDI In Commercial Distribution 🇺🇸 United States

ManaMed Inc

DI: 00810113682488 · Model: PrevenTech · MANAMED INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ManaMed Inc
Primary DI
00810113682488
Version / Model
PrevenTech
Catalog Number
PTECH01
Company Name
MANAMED INC
Labeler DUNS
084042331
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-22
Public Version
1
Public Version Date
2022-08-30
Public Version Status
New
Public Device Record Key
ff98854a-1dd7-46db-b3b3-8c5a7ff1b0f0

Device Description

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.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JOW Sleeve, Limb, Compressible

GMDN Terms

Code Name
44762 Multi-chamber venous compression system garment, single-use

Identifiers

Type ID
Primary 00810113682488

Customer Contacts

Phone
888-508-0712

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius