Identity
- Trade Name
- TRIPORT (ACCELERATOR) FDA UDI
- Generic Name
- Liposuction system cannula, reusable FDA UDI
- Device Name
- Cannula, Triport (Accelerator), specify length, diameter, tip shape and handle/hub FDA UDI
- Model / Reference
- 20120700 FDA UDI
- Description
- Cannula, Triport (Accelerator), specify length, diameter, tip shape and handle/hub FDA UDI
Identifiers
- Catalog Number
- 20-1207-00 FDA UDI
- Primary DI / UDI-DI
- B458201207000 FDA UDI
- FDA Product Code
- GEA FDA UDI
- GMDN Term
- Liposuction system cannula, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Over-the-Counter
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Liposuction system cannula, reusable
Triport (accelerator) by The Wells Johnson Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Liposuction system cannula, reusable.
- SUMMIT MEDICAL — Summit Medical, LLC · Class I
- SUMMIT MEDICAL — Summit Medical, LLC · Class I
- Medco Manufacturing — Medco Manufacturing LLC · Class I
- Double Basket Cannula 2.0 — Möller Medical GmbH · Class I
- Medco Manufacturing — Medco Manufacturing LLC · Class I
- Accelerator III 4mm x 15cm Syringe Cannula — Mentor Texas LP · Class II
- HK Tumescent Infiltration Cannula, (15cm) 6"-14 gauge, Single Use, Box of 10 — HK SURGICAL INC. · Class I
- ORIGINS — Solta Medical, Inc. · Class II
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
- The Wells Johnson Company
Sources (1)
- FDA UDI a36f0baf-2464-4da8-bf1b-848c9a4376b2 34 fields · synced Jun 1, 2026