FDA UDI In Commercial Distribution 🇺🇸 United States

CeramOptec

DI: 04049059519367 · Model: Leonardo® Duster Fiber 200um Reusable, IC · CeramOptec GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CeramOptec
Primary DI
04049059519367
Version / Model
Leonardo® Duster Fiber 200um Reusable, IC
Catalog Number
503200150
Company Name
CeramOptec GmbH
Labeler DUNS
325264513
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-25
Public Version
1
Public Version Date
2025-10-03
Public Version Status
New
Public Device Record Key
c80abd1c-9502-4f9c-89c7-2b0acb36bb19

Device Description

The Leonardo® Duster is intended for incision, excision, resection, ablation, coagulation, hemostasis, and vaporization of soft tissue, with or without an endoscope, in the following indications: urology, lithotripsy, gastroenterological surgery and gynecological surgery.

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
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
36170 General/multiple surgical solid-state laser system

Identifiers

Type ID
Primary 04049059519367

Premarket Submissions

Submission Number Supplement Number
K250504 000