← Back to catalogue
SUB MUCOSAL UPP Electrode
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref TEE731
by Cynosure LLC
Identity
- Trade Name
- SUB MUCOSAL UPP Electrode EUDAMEDFDA UDI
- Generic Name
- Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI
- Device Name
- SUB MUCOSAL UPP Electrode EUDAMEDSUB MUCOSAL UPP(2PK) 70 DEGREE, 1/16" FDA UDI
- Model / Reference
- TEE731 EUDAMEDFDA UDI
- Description
- SUB MUCOSAL UPP(2PK) 70 DEGREE, 1/16" FDA UDI
Identifiers
- Catalog Number
- TEE731 FDA UDI
- Primary DI / UDI-DI
- 00841494104764 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00841494104764 EUDAMED
- FDA Product Code
- JOS FDA UDI
- EMDN Code
- L180601 OPEN ELECTROSURGERY ELECTRODES, REUSABLE EUDAMED
- GMDN Term
- Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
SUB MUCOSAL UPP Electrode by Cynosure, LLC — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00841494104764 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cynosure LLC
- EUDAMED SRN
- US-MF-000010200
- Authorised Representative
- Cynosure B.V. NL-AR-000009566
Sources (2)
- EUDAMED 5693d0e7-9662-4ffd-8055-6b8dcbb4b368 61 fields · synced Jun 18, 2026
- FDA UDI a5e3aea0-9f4a-4795-85e9-ef683cab6470 34 fields · synced May 30, 2026