FDA.reportPublic FDA data

SurgyCut

Primary DI
00810014631967
Brand
SurgyCut
Company
U.S. SURGITECH INC.
Model
790-204-535
Device description
SurgyCut Disposable Hook Scissor Shaft, 5mm/35cm
Published
2019-09-17
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
00810014631950PackageGS110In Commercial Distribution
00810014631967PackageGS1100In Commercial Distribution
00810014631943PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810014631950008100146319508100146319500810014631950
00810014631967008100146319678100146319670810014631967
00810014631943008100146319438100146319430810014631943

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
00810014632612SurgyCut790-120-5452023-06-14
00810014632155SurgyCut790-105-5452023-06-09
00810014632186SurgyCut790-106-5452023-06-09
00810014632216SurgyCut790-107-5452023-06-09

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