FDA UDI In Commercial Distribution 🇺🇸 United States

Applicator VO

DI: 07290016586572 · Model: 20900370BK · POLLOGEN LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Applicator VO
Primary DI
07290016586572
Version / Model
20900370BK
Company Name
POLLOGEN LTD
Labeler DUNS
514905681
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-02
Public Version
3
Public Version Date
2026-04-27
Public Version Status
Update
Public Device Record Key
d482e5de-226c-4b3b-a7e5-158cac65748b

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

GMDN Terms

Code Name
58456 Radio-frequency skin surface treatment/fat liquefaction system control unit

Identifiers

Type ID
Primary 07290016586572

Premarket Submissions

Submission Number Supplement Number
K240999 000
K252576 000