Identity
- Trade Name
- SURG-E-VAC SMOKE EVACUATION SYSTEM FDA UDI
- Generic Name
- Surgical plume evacuation system filter FDA UDI
- Device Name
- SURG-E-VAC 220V SMOKE EVACUATION SYSTEM FDA UDI
- Model / Reference
- SVD220 FDA UDI
- Description
- SURG-E-VAC 220V SMOKE EVACUATION SYSTEM FDA UDI
Identifiers
- Catalog Number
- SVD220 FDA UDI
- Primary DI / UDI-DI
- 00841494104856 FDA UDI
- 510(k) Number
- K983333 FDA UDI
- FDA Product Code
- FYD FDA UDI
- GMDN Term
- Surgical plume evacuation system filter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5070 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical plume evacuation system filter
Surg-E-Vac Smoke Evacuation System by Cynosure, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical plume evacuation system filter.
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- CONMED — Conmed Corporation · Class II
- Neptune — Stryker Corp. · Class II
- VIROSAFE — Conmed Corporation · Class II
- Geiger Smoke Evacuator Filter — DERMATOLOGIC LAB AND SUPPLY, INC. · Class II
Cleared under the same submission
K983333 also covers:
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
- Cynosure, LLC
Sources (1)
- FDA UDI 9893c0d5-e773-4968-afb7-ab01e47eb672 35 fields · synced May 31, 2026