FDA UDI In Commercial Distribution 🇺🇸 United States

AGNES-S

DI: 08800067700019 · Model: AGNES-S · AGNES MEDICAL CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AGNES-S
Primary DI
08800067700019
Version / Model
AGNES-S
Company Name
AGNES MEDICAL CO., LTD.
Labeler DUNS
987426048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-14
Public Version
2
Public Version Date
2026-04-28
Public Version Status
Update
Public Device Record Key
b572a7a7-af5f-4f60-93c1-b318ba3daeac

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
KCW Epilator, High Frequency, Needle-Type

GMDN Terms

Code Name
66285 Intradermal radio-frequency ablation system

Identifiers

Type ID
Primary 08800067700019

Customer Contacts

Storage Conditions

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