FDA UDI In Commercial Distribution 🇺🇸 United States

MASTERPULS®

DI: 07630039101169 · Model: ONE · Storz Medical AG
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MASTERPULS®
Primary DI
07630039101169
Version / Model
ONE
Company Name
Storz Medical AG
Labeler DUNS
481967776
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-16
Public Version
2
Public Version Date
2020-08-20
Public Version Status
Update
Public Device Record Key
05d4dce4-3b7f-483c-9858-ff43d0ff1003

Device Description

The MASTERPULS® ONE is a compressed air-operated ballistic pressure wave generator.

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
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
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
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
47979 Pressure-wave skin contouring system
36560 Hand-held electric massager

Identifiers

Type ID
Primary 07630039101169

Premarket Submissions

Submission Number Supplement Number
K173692 000