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Microincision Tip

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref SST-NModel SFT-S

by Soniquence, LLC

Identity

Trade Name
Microincision Tip EUDAMED
Sp-Tip FDA UDI
Generic Name
Electrosurgical handpiece, single-use FDA UDI
Device Name
Malleable Tip EUDAMED
5mm tip length, 3cm shaft length FDA UDI
Model / Reference
SFT-S EUDAMED
SST-N EUDAMEDFDA UDI
Description
5mm tip length, 3cm shaft length FDA UDI

Identifiers

Catalog Number
SST-N FDA UDI
Primary DI / UDI-DI
00810026181061 EUDAMEDFDA UDI
Basic UDI-DI
0081002618SFT-SKJ EUDAMED
510(k) Number
K183611 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
K0201010301 OPEN ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED
GMDN Term
Electrosurgical handpiece, single-use FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class 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
MRI Safety
MR Unsafe FDA UDI

Microincision Tip 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

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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 12806b2e-fee1-4e77-97c1-c58c82351fdf 61 fields · synced Sep 18, 2026
  • FDA UDI b1c61401-8a86-4c4b-9288-1d2800b589dc 35 fields · synced May 30, 2026