Barrx

Primary DI
10884521189300
Brand
Barrx
Company
Covidien LP
Model
32041-18-01
Device description
360 RFA Balloon Catheter
Published
2016-09-24
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
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
K083711000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K083711000MODIFICATION TO: HALO COAGULATION CATHETER, MODELS 32041-18, 32041-20, 32041-22, 32041-25, 32041-28, 32041-31, 32041-34Barrx Medical, Incorporated2009-02-02GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10884521189300PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088452118930010884521189300

GMDN Terms#

Term, Definition table
TermDefinition
Endoscopic electrosurgical handpiece/electrode, bipolar, single-useA sterile electrosurgical device which consists of a handpiece with mechanical and/or electrical controls, and a bipolar electrode intended to deliver electrosurgical current from a system generator directly to tissues for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery; it is not intended for focal percutaneous ablation. It includes a long thin electrode connected to the handpiece, and may include a lumen for suction/irrigation; it is available in a variety of forms (e.g., forceps, rigid probe with controls). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter18Millimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(508)261-8000Covidien.UDI@covidien.com

Regulatory Flags#

DUNS number
058614483
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00643169694859TrailBlazer™AngledASC-014-0902016-10-22
00643169694866TrailBlazer™AngledASC-014-1352016-10-22
00643169694873TrailBlazer™AngledASC-014-1502016-10-22
00643169694880TrailBlazer™AngledASC-018-0902016-10-22
00643169694897TrailBlazer™AngledASC-018-1352016-10-22
00643169694903TrailBlazer™AngledASC-018-1502016-10-22
00643169694910TrailBlazer™AngledASC-035-0652016-10-22
00643169694927TrailBlazer™AngledASC-035-0902016-10-22
00643169694934TrailBlazer™AngledASC-035-1352016-10-22
00643169694941TrailBlazer™AngledASC-035-1502016-10-22
00763000004804TrailBlazer™ AngledASC-014-0902017-12-22
00763000004811TrailBlazer™ AngledASC-014-1352017-12-22
00763000004828TrailBlazer™ AngledASC-014-1502017-12-22
00763000004835TrailBlazer™ AngledASC-018-0902017-12-22
00763000004842TrailBlazer™ AngledASC-018-1352017-12-22
00763000004859TrailBlazer™ AngledASC-018-1502017-12-22
00763000004866TrailBlazer™ AngledASC-035-0652017-12-22
00763000004873TrailBlazer™ AngledASC-035-0902017-12-22
00763000004880TrailBlazer™ AngledASC-035-1352017-12-22
00763000004897TrailBlazer™ AngledASC-035-1502017-12-22

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00841019123720KirwanKIRWAN SURGICAL PRODUCTS LLCGEI2026-08-19
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