FDA UDI Not in Commercial Distribution 🇺🇸 United States

AcuPulse™ Upgrade Kit 40AES-F to 40AES-R

DI: 07290109142845 · Model: AcuPulse™ Upgrade Kit 40AES-F to 40AES-R · LUMENIS LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AcuPulse™ Upgrade Kit 40AES-F to 40AES-R
Primary DI
07290109142845
Version / Model
AcuPulse™ Upgrade Kit 40AES-F to 40AES-R
Company Name
LUMENIS LTD.
Labeler DUNS
600166524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
5
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
fdcfcc11-d8dd-4dc5-9a9d-8aa54c236af1
Distribution End Date
2023-12-04

Device Description

Additional DM UDI: 07290109144054; 07290109144047; 07290109144078; 07290109144122

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

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 07290109142845
Direct Marking 07290109144061

Customer Contacts

Phone
408-764-3000