Identity
- Trade Name
- SnapEvac EUDAMEDFDA UDI
- Generic Name
- Surgical plume evacuation system tube FDA UDI
- Device Name
- Electrosurgical Accessories EUDAMEDSnapEvac Electrosurgical Pencil Adapter FDA UDI
- Model / Reference
- SNAPEVAC20 EUDAMEDFDA UDI
- Description
- SnapEvac Electrosurgical Pencil Adapter FDA UDI
Identifiers
- Catalog Number
- SNAPEVAC20 FDA UDI
- Primary DI / UDI-DI
- 20845854061807 EUDAMEDFDA UDI
- Basic UDI-DI
- B-20845854061807 EUDAMED
- 510(k) Number
- K230547 FDA UDI
- FDA Product Code
- FYD FDA UDI
- EMDN Code
- K02010107 SMOKE EVACUATION SYSTEMS EUDAMED
- GMDN Term
- Surgical plume evacuation system tube FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 878.5070 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Surgical plume evacuation system tube
SnapEvac by Conmed Corporation — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Surgical plume evacuation system tube.
- Valleylab — Covidien LP · Class II
- BCL Accessories Kit — CairnSurgical Inc · Class IIb
- Surgimedics® — COASTAL LIFE TECHNOLOGIES, INC. · Class I
- SUSI® — Aesculap AG · Class IIa
- Gynex — GYNEX CORPORATION · Class I
- Smoke Tubing — I.C. Medical, Inc. · Class II
- STERILE SURGICAL SCISSORS — Anhui Medfaith Medical Devices Co., Ltd. · Class I
- Bovie — BOVIE MEDICAL CORPORATION · Class II
Cleared under the same submission
K230547 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
Sources (2)
- FDA UDI df291497-f688-4be3-871d-ed88a3230904 36 fields · synced Jul 14, 2026
- EUDAMED ed96a059-3e41-43e8-a3de-eeec3399d5ad 61 fields · synced Jul 14, 2026