FDA UDI In Commercial Distribution 🇺🇸 United States

SHOCKPULSE

DI: 00821925043824 · Model: SPL-SR · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SHOCKPULSE
Primary DI
00821925043824
Version / Model
SPL-SR
Company Name
Gyrus ACMI, LLC
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-24
Public Version
2
Public Version Date
2024-09-02
Public Version Status
Update
Public Device Record Key
37c59a57-25b1-42f7-9ff7-b3c6af5cf834

Device Description

LITHOTRIPSY SYSTEM SHOCKPULSE-SE

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FEO Lithotriptor, Ultrasonic

GMDN Terms

Code Name
37139 Ultrasonic lithotripsy system probe, reusable

Identifiers

Type ID
Primary 00821925043824

Premarket Submissions

Submission Number Supplement Number
K142428 000

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
172 – 230 KiloPascal
Type
Handling Environment Temperature
Temperature Range
270 – 279 Degrees Fahrenheit