FDA UDI In Commercial Distribution 🇺🇸 United States

SHOCKPULSE

DI: 00821925044241 · Model: SPL-PDBX376 · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
SHOCKPULSE
Primary DI
00821925044241
Version / Model
SPL-PDBX376
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
3
Public Version Date
2024-11-18
Public Version Status
Update
Public Device Record Key
b6d76867-5d82-421e-9091-807a17474612

Device Description

LITHOTRIPSY PROBE, STERILE SINGLE USE, ShockPulse-SE 11.3 Fr (3.76 mm) x 396 mm (3/PK)

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FEO Lithotriptor, Ultrasonic

GMDN Terms

Code Name
60703 Ultrasonic lithotripsy system probe, single-use

Identifiers

Type ID
Package 00821925043763
Primary 00821925044241