FDA.reportPublic FDA data

SurgyCut

Primary DI
00810014632612
Brand
SurgyCut
Company
U.S. SURGITECH INC.
Model
790-120-545
Device description
SurgyCut Straight Blade Hand Control Electrode, 5mm/45cm
Published
2023-06-14
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810014632612PackageGS110In Commercial Distribution
00810014632629PackageGS110In Commercial Distribution
00810014632605PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810014632612008100146326128100146326120810014632612
00810014632629008100146326298100146326290810014632629
00810014632605008100146326058100146326050810014632605

GMDN Terms#

Term, Definition table
TermDefinition
Endoscopic electrosurgical electrode, monopolar, single-useA sterile, invasive, distal component of an electrosurgical assembly intended to deliver electrosurgical current in a monopolar configuration (i.e., used with a patient contact return electrode) to tissues for cutting/coagulation/ablation during endoscopic (e.g., laparoscopic, arthroscopic) surgery. It is available in a variety of forms (e.g., exchangeable electrode for electrosurgical forceps, rigid electrode, flexible endoscopic probe) which may include a lumen for suction/irrigation. It does not include a handpiece or housing and has no electrical or mechanical controls (e.g., does not include ring-handles); it is not intended for gas-enhanced electrosurgery. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
142007082
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
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
00810014639901SurgyCut790SCBF012024-10-10
00810014636832SurgyPad780SP92024-10-10
10810014639908SurgyCut790SCBF012024-10-10
00810014639918SurgyCut790SCGF12024-10-10
00810014631820SurgyCut790-200-535790-200-5352019-03-05
00810014631851SurgyCut790-201-535790-201-5352019-03-20
00810014631882SurgyCut790-202-535790-202-5352019-03-05
00810014631912SurgyCut790-203-535790-203-5352019-03-20
00810014631943SurgyCut790-204-5352019-09-17
00810014632841SurgyCut790-200-5452023-06-09
00810014631974SurgyCut790-205-5352019-12-03
00810014632872SurgyCut790-201-5452019-10-22
00810014635736SurgyFoam780SP12023-07-31
00810014632575SurgyCut790-119-5452023-06-14
00810014632605SurgyCut790-120-5452023-06-14
00810014632582SurgyCut790-119-5452023-06-14
00810014632155SurgyCut790-105-5452023-06-09
00810014632186SurgyCut790-106-5452023-06-09
00810014632216SurgyCut790-107-5452023-06-09
00810014632339SurgyCut790-111-5452023-06-09

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