FDA UDI
In Commercial Distribution
🇺🇸 United States
EndyMed PRO Intensif Handpiece
DI: 07290016814200
·
Model: Intesif Handpiece
·
ENDYMED MEDICAL LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- EndyMed PRO Intensif Handpiece
- Primary DI
- 07290016814200
- Version / Model
- Intesif Handpiece
- Catalog Number
- ND_PRD00185
- Company Name
- ENDYMED MEDICAL LTD
- Labeler DUNS
- 531958689
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-12-31
- Public Version
- 3
- Public Version Date
- 2023-11-21
- Public Version Status
- Update
- Public Device Record Key
- 9c9fe5b9-56a7-4549-8e7d-cd4d7a6de2b0
Device Description
The Intensif applicator is intended for use in dermatologic and general surgical procedure for electrocoagulation nd hemostasis
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
- No
- 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 |
| OUH | Skin Resurfacing Rf Applicator | General, Plastic Surgery | 878.4400 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 61216 | Cosmetic micro-needling electronic handpiece, professional | A hand-held, electrically-powered device intended to be used in combination with a micro-needle cartridge (which contains micro-needles) to create high-density minute skin punctures to stimulate tissue regeneration and improve the appearance of the skin as part of collagen induction therapy (CIT). It includes controls to allow for treatment adjustments (e.g., puncture depth, frequency); a disposable micro-needle cartridge may be included. It is intended for clinical use by a healthcare provider to treat stretch marks, acne scarring, hyperpigmentation, wrinkles, and/or hair loss; it is not intended for energy-based skin treatment. This is a reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 07290016814200 | GS1 |
Customer Contacts
- Phone
- 1-855-363-9633
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K130501 | 000 |