Identity
- Trade Name
- Symmetry Rhoton® FDA UDI
- Generic Name
- Open-surgery dissector FDA UDI
- Device Name
- Rhoton® Dissector, Teardrop, Etched Label #15, Straight, 3 mm Tip, 7 1/2 in, 191 mm FDA UDI
- Model / Reference
- 80-1679 FDA UDI
- Description
- Rhoton® Dissector, Teardrop, Etched Label #15, Straight, 3 mm Tip, 7 1/2 in, 191 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00887482031377 FDA UDI
- FDA Product Code
- GDI FDA UDI
- GMDN Term
- Open-surgery dissector 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 3 Millimeter FDA UDILength — 7.5 Inch FDA UDI
Category: Open-surgery dissector
Symmetry Rhoton® by Symmetry Surgical Inc. — 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
- Symmetry Surgical Inc.
Sources (1)
- FDA UDI ae1b362a-e747-4934-9312-8e92bd11b30a 35 fields · synced Jun 8, 2026