Identity
- Trade Name
- Symmetry Surgical RHOTON FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
- Device Name
- Rhoton Suction Tube; Neuro; Curved Up; 10 Fr; 5 1/8 in (130 mm) Working Length FDA UDI
- Model / Reference
- 58-6340 FDA UDI
- Description
- Rhoton Suction Tube; Neuro; Curved Up; 10 Fr; 5 1/8 in (130 mm) Working Length FDA UDI
Identifiers
- Catalog Number
- 58-6340 FDA UDI
- Primary DI / UDI-DI
- 00887482104125 FDA UDI
- FDA Product Code
- JOL FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 5.125 Inch FDA UDICatheter Gauge — 10 French FDA UDI
Category: Surgical/emergency suction cannula, non-illuminating, reusable
Symmetry Surgical RHOTON by Symmetry Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Symmetry Surgical Inc.
Sources (1)
- FDA UDI 1a2eb05f-d063-41ab-866d-ff178fc8faed 36 fields · synced May 30, 2026