FDA UDI In Commercial Distribution 🇺🇸 United States

AcuPulse™ Upgrade Kit 30 to 30ST

DI: 07290109142876 · Model: AcuPulse™ Upgrade Kit 30 to 30ST · LUMENIS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcuPulse™ Upgrade Kit 30 to 30ST
Primary DI
07290109142876
Version / Model
AcuPulse™ Upgrade Kit 30 to 30ST
Company Name
LUMENIS LTD.
Labeler DUNS
600166524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a6a42761-4b27-4f2e-b44f-1831effe190a

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 07290109142876

Customer Contacts

Phone
408-764-3000

Premarket Submissions

Submission Number Supplement Number
K100415 000