FDA UDI
In Commercial Distribution
🇺🇸 United States
AGNES
DI: 18800067700009
·
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
- 18800067700009
- 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
- e2e7cce7-f5f3-4356-bd2c-d9e1ac4c5d25
Device Description
This is 1 set with following device AGNES: 1EA, GA-B: 10EA, GA-C: 10EA, GA-E: 10EA, GA-F1A: 10EA, GA-F1B: 10EA, GA-I: 10EA, GA-IL: 10EA, GA-S: 10EA, GA-SL: 10EA GA-W3A: 10EA, GA-F3A: 10EA, GA-W3B: 10EA AG-CN18G: 10EA, AG-CN19G: 10EA, AG-CN20G: 10EA, AG-CN21G: 10EA, AG-CN23G: 10EA
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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | General, Plastic Surgery | 878.4400 | 2 |
| KCW | Epilator, High Frequency, Needle-Type | General, Plastic Surgery | 878.5350 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 66285 | Intradermal radio-frequency ablation system | An assembly of devices designed to apply radio-frequency (RF) energy to heat the dermal layer of the skin (e.g., the sebaceous glands) [invasive] for ablation (e.g., thermolysis) during an aesthetic procedure (e.g., acne treatment). It primarily consists of an electrically-powered control unit intended to produce and regulate the RF energy, and a connected monopolar RF applicator (probe) to deliver the RF energy to the skin; it may in addition include a bipolar (noninvasive) RF applicator. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 18800067700009 | GS1 |
Customer Contacts
- Phone
- +823180209717
- [email protected]
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