FDA UDI In Commercial Distribution 🇺🇸 United States

Flowpresso Compression Device

DI: 09413000135374 · Model: LCD10 · MEDELLA HEALTH LIMITED
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Flowpresso Compression Device
Primary DI
09413000135374
Version / Model
LCD10
Company Name
MEDELLA HEALTH LIMITED
Labeler DUNS
671444392
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-16
Public Version
1
Public Version Date
2025-10-24
Public Version Status
New
Public Device Record Key
37567e23-88d9-463b-8449-402a2c6de000

Device Description

The Flowpresso Device combines heat and compression therapy. Flowpresso is intended to treat post traumatic and post-surgical medical and/or surgical conditions for which localized thermal therapy are indicated.

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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IRP Massager, Powered Inflatable Tube
IRT Pad, Heating, Powered

GMDN Terms

Code Name
10969 Intermittent venous compression system

Identifiers

Type ID
Primary 09413000135374

Customer Contacts

Phone
+64221913672

Premarket Submissions

Submission Number Supplement Number
K223729 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
33 – 122 Degrees Fahrenheit