FDA UDI In Commercial Distribution 🇺🇸 United States

AGNES

DI: 08800067700002 · Model: AGNES · AGNES MEDICAL CO., LTD.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AGNES
Primary DI
08800067700002
Version / Model
AGNES
Company Name
AGNES MEDICAL CO., LTD.
Labeler DUNS
695070346
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-14
Public Version
1
Public Version Date
2023-07-24
Public Version Status
New
Public Device Record Key
743a42ed-2dd3-4050-a344-b9e2dbca7959

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
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
KCW Epilator, High Frequency, Needle-Type

GMDN Terms

Code Name
66285 Intradermal radio-frequency ablation system

Identifiers

Type ID
Primary 08800067700002

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K203013 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 80 Percent (%) Relative Humidity