Identity
- Trade Name
- Symmetry Smith FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
- Device Name
- Symmetry® Retractor; Smith Nerve Root Suction; 5 1/2 in Shaft; 10 in FDA UDI
- Model / Reference
- 58-5000 FDA UDI
- Description
- Symmetry® Retractor; Smith Nerve Root Suction; 5 1/2 in Shaft; 10 in FDA UDI
Identifiers
- Catalog Number
- 58-5000 FDA UDI
- Primary DI / UDI-DI
- 00887482103074 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, non-illuminating, 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 10 Inch FDA UDIShaft Length — 5.5 Inch FDA UDI
Category: Surgical/emergency suction cannula, non-illuminating, reusable
Symmetry Smith 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 e8306cf3-f0de-4be6-86aa-964319cdf64b 36 fields · synced May 30, 2026