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Bipolar Forceps

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref SBF-013-10Model SDTFQM-40

by Soniquence, LLC

Identity

Trade Name
Bipolar Forceps EUDAMEDFDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
Bipolar Wand EUDAMED
Bipolar Forceps reusable, Bayonet, 7 3/4", 1.0mm tip FDA UDI
Model / Reference
SDTFQM-40 EUDAMED
SBF-013-10 EUDAMEDFDA UDI
Description
Bipolar Forceps reusable, Bayonet, 7 3/4", 1.0mm tip FDA UDI

Identifiers

Catalog Number
SBF-013-10 FDA UDI
Primary DI / UDI-DI
00810026181818 EUDAMEDFDA UDI
Basic UDI-DI
0081002618SDTFQM-40TQ EUDAMED
Direct Marketing DI
00810026181818 EUDAMED
510(k) Number
K964176 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L180401 OPEN ELECTROSURGERY FORCEPS, REUSABLE EUDAMED
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable 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

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Bipolar Forceps by Soniquence, LLC — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, reusable.

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 3b5e3dee-41cf-40c2-bea5-7ca762974ae7 61 fields · synced Jun 19, 2026
  • FDA UDI a11af166-9ba3-474f-baff-b96ce23ff887 35 fields · synced May 30, 2026