FDA UDI In Commercial Distribution 🇺🇸 United States

PressureMate Compression Assist Device

DI: 10815614020064 · Model: 3201 · SEMLER TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PressureMate Compression Assist Device
Primary DI
10815614020064
Version / Model
3201
Catalog Number
130-0201-00
Company Name
SEMLER TECHNOLOGIES, INC.
Labeler DUNS
042075700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
ef63ab83-fecc-475a-b6a0-4894376fbe48

Device Description

The PressureMate Compression Assist Device is designed to enhance comfort for the practitioner and the patient when applying external compression of the femoral artery. Practitioners apply external pressure with PressureMate in much the same way that they would when applying manual pressure. PressureMate is comprised of a non-sterile, reusable handle and a sterile, disposable SuperComfort Disc (Model 5303 or 5305) to aid in the practice of manual compression. The Model 3201 is of 23 oz. weighted stainless steel construction.

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXC Clamp, Vascular

GMDN Terms

Code Name
46367 Femoral artery compression system, manual, reusable

Identifiers

Type ID
Primary 10815614020064

Premarket Submissions

Submission Number Supplement Number
K090286 000