FDA.reportPublic FDA data

CATHAY

Primary DI
16959006300397
Brand
CATHAY
Company
CATHAY MANUFACTURING CORP.
Model
GP202D-T
Device description
Horizontal Monopolar Adult Grounding Pad
Published
2019-06-05
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
false
OTC
false
Sterile
false
Single use
true

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
K130027000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K130027000DISPOSABLE NEUTRAL ELECTRODE GP202Cathay Manufacturing Corp.2013-08-22GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16959006300397PackageGS18In Commercial Distribution
06959006300390PrimaryGS10
26959006300394Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1695900630039716959006300397
06959006300390069590063003906959006300390
2695900630039426959006300394

GMDN Terms#

Term, Definition table
TermDefinition
Electrosurgical return electrode, single-use, non-sterileA non-sterile dispersive conductor intended to be fastened to a patient and connected to an electrosurgical/radio-frequency ablation system generator, to allow return of electrical current from the patient to the generator during an electrosurgical procedure. It has a large surface area and is fastened to the patient's body typically where the greatest surface area can be covered in closest proximity to the surgical site. It may or may not include a return cable(s). This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+862157878328176541381@qq.com

Regulatory Flags#

DUNS number
421287342
Device count
25
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06959006303315AcuZoneAcuZone-40-2x4pigtail electrodes2020-11-13
06959006303322AcuZoneAcuZone-44-2x2 pigtail electrodes2020-11-13
06959006303339AcuZoneAcuZone-40-2x2SNAP electrodes2020-11-13
06959006303308AngelAngel-40-2x2 pigtails electrodes2020-11-13
06959006300437CathayGP202S-AB2024-06-19
06959006300444CathayGP202D-AB2024-06-19
06959006300451CathayGP202S-PB2024-06-19
06959006300468CathayGP202D-PB2024-06-19
06959006300475CathayGP202S-IB2024-06-19
06959006300482CathayGP202D-IB2024-06-19
06959006300505CathayGP202D-TB2023-10-08
06959006300772CathayGP202S-PCB2023-10-08
06959006300789CathayGP202D-PCB2023-10-08
06959006300819CathayGP202S-TCB2023-10-08
06959006300826CathayGP202D-TCB2023-10-08
06959006302981CathayCP10012023-10-08
06959006304404CathayGP202S-TCB2023-10-08
06959006304411CathayGP202D-TCB2023-10-08
06959006300499CathayGP202S-TB2023-10-08
16959006300502CathayGP202D-TB2023-10-08

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00840319759073Hayden MedicalHayden Medical, Inc.GEI2026-06-04
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08809306764164VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764171VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764188VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
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