FDA UDI In Commercial Distribution 🇺🇸 United States

Zemits OxiVelour

DI: 00860010841167 · Model: 1 · Advance-Esthetic LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zemits OxiVelour
Primary DI
00860010841167
Version / Model
1
Catalog Number
123621
Company Name
Advance-Esthetic LLC
Labeler DUNS
043911204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-27
Public Version
1
Public Version Date
2024-02-05
Public Version Status
New
Public Device Record Key
939f166b-ff24-4193-9e8e-9bc229fa45ab

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GFE Brush, Dermabrasion, Powered

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 00860010841167

Customer Contacts

Phone
8889993996