FDA UDI In Commercial Distribution 🇺🇸 United States

DermalInfusion Pro

DI: 00816417021879 · Model: A1002 · Zeltiq Aesthetics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DermalInfusion Pro
Primary DI
00816417021879
Version / Model
A1002
Catalog Number
A1002
Company Name
Zeltiq Aesthetics, Inc.
Labeler DUNS
809152916
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-19
Public Version
1
Public Version Date
2021-03-29
Public Version Status
New
Public Device Record Key
820d5e3e-826f-4eca-ab57-a1bbe83b124e

Device Description

Dermalinfusion Pro

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
Yes
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
GFE Brush, Dermabrasion, Powered

GMDN Terms

Code Name
32388 Dermabrasion brush, rotary

Identifiers

Type ID
Primary 00816417021879

Customer Contacts

Phone
888-935-8471