Identity
- Trade Name
- Bi-Turbinate Probe EUDAMEDFDA UDI
- Generic Name
- Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
- Device Name
- Bipolar Wand EUDAMEDBi-Turbinate Probe (Bayonet) Disposable 17.5cm (1 pc) FDA UDI
- Model / Reference
- SDTFQM-40 EUDAMEDSTURB-D EUDAMEDFDA UDI
- Description
- Bi-Turbinate Probe (Bayonet) Disposable 17.5cm (1 pc) FDA UDI
Identifiers
- Catalog Number
- STURB-D FDA UDI
- Primary DI / UDI-DI
- 00810026180569 EUDAMEDFDA UDI
- Basic UDI-DI
- 0081002618SDTFQM-40TQ EUDAMED
- 510(k) Number
- K002257 FDA UDI
- FDA Product Code
- GEI FDA UDI
- EMDN Code
- K0201011201 OPEN ELECTROSURGERY PROBES, SINGLE-USE EUDAMED
- GMDN Term
- Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Market of Registration
- France 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
MR Unsafe FDA UDI
Bi-Turbinate Probe by Soniquence, LLC — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0081002618SDTFQM-40TQ | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Soniquence, LLC
- EUDAMED SRN
- US-MF-000029810
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 435caff1-0583-4b45-bfc1-6b3724e9e02e 61 fields · synced Jul 10, 2026
- FDA UDI f0069308-75ac-410f-b5a2-b139e4ba08d3 35 fields · synced May 30, 2026