FDA UDI In Commercial Distribution 🇺🇸 United States

4MM Handpiece Assembly

DI: 00817495020495 · Model: 7122-00-1101 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
4MM Handpiece Assembly
Primary DI
00817495020495
Version / Model
7122-00-1101
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2022-10-12
Public Version Status
Update
Public Device Record Key
4129a6ca-d147-487a-a934-d843585af6f6

Device Description

Hand-piece Assembly

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
45221 Dermatological laser beam guiding handpiece

Identifiers

Type ID
Primary 00817495020495
Previous 08174950200499

Customer Contacts

Phone
800-735-2737

Premarket Submissions

Submission Number Supplement Number
K081324 000