LAP CHOLE KIT

Primary DI
30607915127047
Brand
LAP CHOLE KIT
Company
APPLIED MEDICAL RESOURCES CORPORATION
Model
K2209
Device description
Kit Contains: CA090, DIRECT DRIVE® LCA 3/BXCTB73, 12x100 Kii® SH BLD ZTHR 6/BXCTS02, 5x100 Kii® SLEEVE ZTHR 12/BXCTS22, 12x100 Kii® SLEEVE ZTHR 12/BXC6001, 5mmX33cm PROB/VALV DUAL BAG 12/BXCTB03, 5x100 Kii® SH BLD ZTHR 6/BXCB030, 5mmx35cm EPIX® LAPA SCISSOR, 10/BXC2201, 120MM INSUFF NEEDLE XE, 20/BX
Published
2015-10-16
Public version status
Update
Distribution status
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
FHFSystem, Evacuator, Fluid
FZPClip, Implantable
GCJLaparoscope, General & Plastic Surgery
HETLaparoscope, Gynecologic (And Accessories)
MDMInstrument, Manual, Surgical, General Use

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FHFSystem, Evacuator, FluidGastroenterology, Urology2
FZPClip, ImplantableGeneral, Plastic Surgery2
GCJLaparoscope, General & Plastic SurgeryGastroenterology, Urology2
HETLaparoscope, Gynecologic (And Accessories)Obstetrics/Gynecology2
MDMInstrument, Manual, Surgical, General UseGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
30607915127047PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
3060791512704730607915127047

GMDN Terms#

Term, Definition table
TermDefinition
Spring-loaded pneumoperitoneum needle, single-useA slender, sharply-pointed metal tube designed to introduce or remove gas from the peritoneal cavity as a therapeutic or surgical/radiological procedural method. It is often inserted into the peritoneal cavity for the purpose of insufflation [e.g., with carbon dioxide (CO2)] to establish pneumoperitoneum prior to abdominal endoscopy. It is equipped with a spring-loaded, round-tipped obturator that extends from the tube when the device does not encounter resistance (i.e., when the cavity has been reached) to prevent damage from the sharp point. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1.949.713.8300contact@appliedmedical.com

Regulatory Flags#

DUNS number
187129135
Device count
1
Kit
true
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

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