FDA UDI In Commercial Distribution 🇺🇸 United States

Derma Genesis Infusion

DI: 00818257022122 · Model: D11-0358-101 · GENESIS BIOSYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Derma Genesis Infusion
Primary DI
00818257022122
Version / Model
D11-0358-101
Catalog Number
D11-0358-101
Company Name
GENESIS BIOSYSTEMS, INC.
Labeler DUNS
067933700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-24
Public Version
1
Public Version Date
2023-08-01
Public Version Status
New
Public Device Record Key
28aa43f9-2c7a-4235-b27b-828279a5a943

Device Description

Multi Modality Micro-Exfolaition system

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
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
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 00818257022122

Customer Contacts

Phone
9723157888