FDA.reportPublic FDA data

ARCO-MULTIFUNCTIONAL-INSTRUMENT

Primary DI
04250321508167
Brand
ARCO-MULTIFUNCTIONAL-INSTRUMENT
Company
Söring GmbH
Model
53-027
Device description
Argon instrument, hand activation
Published
2016-09-17
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K993265000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K993265000SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600Soring GmbH Medizintechnik1999-10-22GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04250321508167PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04250321508167042503215081674250321508167

GMDN Terms#

Term, Definition table
TermDefinition
Neutral plasma surgical system handpieceA sterile hand-held instrument used with a neutral plasma surgical system control unit to coagulate, cut, and/or vaporize/ablate tissue during open and/or laparoscopic surgery. Inert argon (Ar) gas is excited (ionized) in the instrument by a series of internal bipolar electrodes to generate plasma (atomic ions and free electrons) which emerges from the tip of the handpiece in a stream to release kinetic and thermal energy upon contact with tissue. Operation is regulated using a hand-control on the instrument or via a connected foot-switch. The instrument is typically in the form of a pen/pencil with attached cables for connection to the control unit. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
844 476 7464UDI-inquiry@soering.com

Regulatory Flags#

DUNS number
322238346
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04250321528325NA700S03162016-09-17
04250321519965UAW Instrument97-10297-1022023-06-12
04250321519989UAW Instrument97-10497-1042023-06-12
04250321520008UAW Instrument97-11297-1122023-06-12
04250321523535UAW Instrument97-10397-1032023-06-12
04250321532612SONOCA 185S185-000B-FLS185-000B-FL2023-06-12
04250321519217ENP92-0302016-09-17
04250321527588NA770S00012016-09-17
04250321532315ARCO 300068-000B-FL2016-09-17
04250321532346BCC 140B140-0000B-FL2016-09-17
04250321532483MBC 200M200-0000B-FL2016-09-17
04250321532575MBC 601 UAM88-000B-UAM-FL2016-09-17
04250321522897NA300K00112016-09-17
04250321522903NA300K00132016-09-17
04250321512591NA612K0037-502016-09-17
04250321512652NA612K0039-502016-09-17
04250321519125Pen91-0212016-09-17
04250321519637LUD94-0542016-09-17
04250321519699NA94-106-HF2016-09-17
04250321523245NA612K0038-502016-09-17

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