Identity
- Trade Name
- JetPeel FDA UDI
- Generic Name
- Liquid-jet skin surface treatment system applicator, reusable FDA UDI
- Model / Reference
- Blue Line Magic HP FDA UDI
Identifiers
- Catalog Number
- JTD-005 FDA UDI
- Primary DI / UDI-DI
- 07290014242722 FDA UDI
- FDA Product Code
- GFE FDA UDI
- GMDN Term
- Liquid-jet skin surface treatment system applicator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Liquid-jet skin surface treatment system applicator, reusable
JetPeel by Tav - Tech Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Liquid-jet skin surface treatment system applicator, reusable.
- JetPeel — TAV - TECH LTD · Class I
- JetPeel — TAV - TECH LTD · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tav - Tech Ltd
Sources (1)
- FDA UDI 3c3e5bab-07aa-4318-a0fe-9ed8136a505e 34 fields · synced May 30, 2026