FDA UDI In Commercial Distribution 🇺🇸 United States

AcuTip 500

DI: 00816722022103 · Model: AcuTip 500 · CUTERA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AcuTip 500
Primary DI
00816722022103
Version / Model
AcuTip 500
Company Name
CUTERA, INC.
Labeler DUNS
041071643
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2022-12-01
Public Version Status
Update
Public Device Record Key
e99735e7-3779-466e-b4db-b7484c569c89

Device Description

AcuTip 500 IPL Handpiece

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
45222 Light-energy skin surface treatment system applicator

Identifiers

Type ID
Primary 00816722022103

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K050047 000