FDA UDI In Commercial Distribution 🇺🇸 United States

CeramOptec

DI: 04049059301092 · Model: Leonardo® DUAL 200 · CeramOptec GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CeramOptec
Primary DI
04049059301092
Version / Model
Leonardo® DUAL 200
Company Name
CeramOptec GmbH
Labeler DUNS
325264513
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-15
Public Version
1
Public Version Date
2024-11-25
Public Version Status
New
Public Device Record Key
478c2bdb-5263-48a4-bac8-677dcc0954eb

Device Description

Indicated for use in general surgical applications for incision, excision, ablation, cutting, vaporization, hemostasis, and coagulation of soft tissue contact or non-contact, open or closed endoscopic applications where incision, tissue dissection, excision of external tumors and lesions, complete or partial resection of internal organs, tumors and lesions, tissue vaporization, hemostasis and/or coagulation may be indicated.

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 04049059301092