FDA UDI
In Commercial Distribution
🇺🇸 United States
Dermalux
DI: 05060762460011
·
Model: Tri-Wave MD MKII
·
AESTHETIC TECHNOLOGY LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Dermalux
- Primary DI
- 05060762460011
- Version / Model
- Tri-Wave MD MKII
- Catalog Number
- 1000021
- Company Name
- AESTHETIC TECHNOLOGY LTD
- Labeler DUNS
- 218753736
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-09-02
- Public Version
- 2
- Public Version Date
- 2026-02-11
- Public Version Status
- Update
- Public Device Record Key
- b218ad29-7124-4064-84c8-379fd5973fe4
Device Description
4-Pod LED phototherapy device.
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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | General, Plastic Surgery | 878.4810 | 2 |
| ILY | Lamp, Infrared, Therapeutic Heating | Physical Medicine | 890.5500 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 62202 | Blue/red/infrared phototherapy lamp | A portable, electrically-powered device designed to emit blue light, red light, and infrared radiation (heating effect) for phototherapy treatment of mild skin disorders (e.g., mild acne), superficial skin wounds, musculoskeletal symptoms (e.g., pain, spasm, stiffness), and/or for cosmetic skin rejuvenation. It may have various designs (e.g., hand-held, book-like, flexible pad for adapting to body areas) and is intended for use in the home or a clinical setting. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 05060762460011 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K240222 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 679.7 | Millimeter | |
| Height | 1087.4 | Millimeter | |
| Width | 517.7 | Millimeter | |
| Weight | 55 | Kilogram |