FDA UDI In Commercial Distribution 🇺🇸 United States

DUOLITH®

DI: 07630039101404 · Model: SD1 Tower · Storz Medical AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DUOLITH®
Primary DI
07630039101404
Version / Model
SD1 Tower
Catalog Number
19880.0005
Company Name
Storz Medical AG
Labeler DUNS
481967776
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-29
Public Version
1
Public Version Date
2021-07-07
Public Version Status
New
Public Device Record Key
64ac8754-85ce-421e-9a1b-565aa3783db7

Device Description

The device is indicated for extracorporeal shock wave treatment.

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
MR Unsafe
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
NBN Generator, Shock-Wave, For Pain Relief
PZL Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
47995 Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system

Identifiers

Type ID
Primary 07630039101404

Premarket Submissions

Submission Number Supplement Number
K173692 000
K202112 000
P080028 001