FDA UDI In Commercial Distribution 🇺🇸 United States

TriLift

DI: 07290016586534 · Model: TriLift · POLLOGEN LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TriLift
Primary DI
07290016586534
Version / Model
TriLift
Catalog Number
30020000BK
Company Name
POLLOGEN LTD
Labeler DUNS
514905681
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-13
Public Version
2
Public Version Date
2024-02-12
Public Version Status
Update
Public Device Record Key
5b07004a-c3ea-4b01-a4f0-7e5e2a3cdb39

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
Yes
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58455 Radio-frequency skin surface treatment system applicator

Identifiers

Type ID
Primary 07290016586534

Premarket Submissions

Submission Number Supplement Number
K173503 000
K200545 000
K232903 000