FDA UDI In Commercial Distribution 🇺🇸 United States

Digital AcuBlade™ Upgrade kit for UltraPulse® SurgiTouch™

DI: 07290109142142 · Model: Kit for up to 007-xxxx, 110V · LUMENIS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Digital AcuBlade™ Upgrade kit for UltraPulse® SurgiTouch™
Primary DI
07290109142142
Version / Model
Kit for up to 007-xxxx, 110V
Company Name
LUMENIS LTD.
Labeler DUNS
600166524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-30
Public Version
4
Public Version Date
2021-10-21
Public Version Status
Update
Public Device Record Key
3995c914-5ca3-4c46-a3eb-bfd69f2eb18a

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
No
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
17774 General/multiple surgical solid-state/carbon dioxide laser system

Identifiers

Type ID
Primary 07290109142142

Customer Contacts

Phone
408-764-3000