FDA UDI
In Commercial Distribution
🇺🇸 United States
7.5mm GlideSafe HP (3) and Cable
DI: 00841494108328
·
Model: P275HPD
·
Cynosure, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- 7.5mm GlideSafe HP (3) and Cable
- Primary DI
- 00841494108328
- Version / Model
- P275HPD
- Company Name
- Cynosure, LLC
- Labeler DUNS
- 780318028
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-09-17
- Public Version
- 2
- Public Version Date
- 2023-01-11
- Public Version Status
- Update
- Public Device Record Key
- 01617ff7-0452-48e3-a7e0-b58f8cce7a8d
Device Description
7.5mm GlideSafe HP (3) and Cable
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
- No
- Has Lot/Batch Number
- Yes
- 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 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 45214 | Radio-frequency skin contouring system applicator, monopolar | A monopolar handpiece that is part of a skin contouring system that uses radio-frequency (RF) energy to provide a capacitively coupled electrical connection for the transfer of radiated energy through a patient's skin in deep heat-mediated skin modification. The current passes from this device to an indifferent return electrode placed on the patient. This device is connected to a generator and is applied by the practitioner or staff directly to the area to be treated. This is a reusable device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00841494108328 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K102698 | 000 |