Identity
- Trade Name
- STANDARD CANNULA SET FDA UDI
- Generic Name
- Liposuction system cannula, reusable FDA UDI
- Device Name
- Cannula Set, Standard Cannula Set, contains: -3-Port Radial (Mercedes) 3mm x 25cm on 7/8" tip base w/vent (P/N: 20-1205-00) -3-Port Radial (Mercedes) 3mm x 15cm on 7/8" tip base w/vent (P/N: 20-1205-00) -Triport (Accelerator) 4mm x 25cm on 7/8" tip base w/vent (P/N: 20-1207-00) -Triport (Accelerator) 3mm x 25cm on 7/8" tip base w/vent (P/N: 20-1207-00) -Becker Grater Round 3mm x 25cm on 7/8" tip base (P/N: 20-1230-00) -Puente Tornado 2.7mm x 17cm on 7/8" tip base w/vent (P/N: 20-1236-00) -Puente Tornado 2mm x 15cm on 7/8" tip base w/vent (P/N: 20-1236-00) -1" Delrin Handle x2ea (P/N: 20-0005-00) FDA UDI
- Model / Reference
- 20105800 FDA UDI
- Description
- Cannula Set, Standard Cannula Set, contains: -3-Port Radial (Mercedes) 3mm x 25cm on 7/8" tip base w/vent (P/N: 20-1205-00) -3-Port Radial (Mercedes) 3mm x 15cm on 7/8" tip base w/vent (P/N: 20-1205-00) -Triport (Accelerator) 4mm x 25cm on 7/8" tip base w/vent (P/N: 20-1207-00) -Triport (Accelerator) 3mm x 25cm on 7/8" tip base w/vent (P/N: 20-1207-00) -Becker Grater Round 3mm x 25cm on 7/8" tip base (P/N: 20-1230-00) -Puente Tornado 2.7mm x 17cm on 7/8" tip base w/vent (P/N: 20-1236-00) -Puente Tornado 2mm x 15cm on 7/8" tip base w/vent (P/N: 20-1236-00) -1" Delrin Handle x2ea (P/N: 20-0005-00) FDA UDI
Identifiers
- Catalog Number
- 20-1058-00 FDA UDI
- Primary DI / UDI-DI
- B458201058000 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
Standard Cannula Set by The Wells Johnson Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- The Wells Johnson Company
Sources (1)
- FDA UDI d10ffb28-af76-484a-b9be-f8cc9d541145 34 fields · synced Jun 8, 2026