FDA.reportPublic FDA data

Insufflation-needle acc. to Veress

Primary DI
04048223008331
Brand
Insufflation-needle acc. to Veress
Company
Pajunk GmbH Medizintechnologie
Model
1206-00150
Catalog number
1206-00150
Device description
Insufflation-needle acc. to Veress 0,083 x 5,905 inch
Published
2016-09-27
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HETLAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HETLaparoscope, Gynecologic (And Accessories)Obstetrics/Gynecology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K062097000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K062097000VERESS CANNULA AND MODULAR VERESS CANNULAPAJUNK GmbH Medizintechnologie2006-10-13HET

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04048223008331PrimaryGS10
04048223077498PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04048223008331040482230083314048223008331
04048223077498040482230774984048223077498

GMDN Terms#

Term, Definition table
TermDefinition
Spring-loaded pneumoperitoneum needle, reusableA 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 reusable device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Humidity10 Percent (%) Relative Humidity65 Percent (%) Relative Humidity
Storage Environment Temperature10 Degrees Celsius30 Degrees Celsius

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(888)972-5865info@pajunk-usa.com
+1 770-493-6832info@pajunk-usa.com

Regulatory Flags#

DUNS number
317654283
Device count
1
Lot or batch
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04048223122655Tuohy II1170-6I0911170-6I0912026-10-22
04048223122679Tuohy II1170-6K0811170-6K0812026-10-22
04048223122693Tuohy II1170-6K0911170-6K0912026-10-22
04048223122716Tuohy II1170-6K1201170-6K1202026-10-22
04048223122730Tuohy II1170-6M0811170-6M0812026-10-22
04048223122754Tuohy II1170-6M0911170-6M0912026-10-22
04048223122792Tuohy II1170-6O0811170-6O0812026-10-22
04048223122815Tuohy II1170-6O0911170-6O0912026-10-22
04048223122877Tuohy II NRFit1176-6I0911176-6I0912026-10-22
04048223122891Tuohy II NRFit1176-6K0811176-6K0812026-10-22
04048223122914Tuohy II NRFit1176-6K0911176-6K0912026-10-22
04048223122938Tuohy II NRFit1176-6K1201176-6K1202026-10-22
04048223122952Tuohy II NRFit1176-6M0811176-6M0812026-10-22
04048223122976Tuohy II NRFit1176-6M0911176-6M0912026-10-22
04048223122990Tuohy II NRFit1176-6M1201176-6M1202026-10-22
04048223123010Tuohy II NRFit1176-6O0811176-6O0812026-10-22
04048223123034Tuohy II NRFit1176-6O0911176-6O0912026-10-22
04048223124574Tuohy II NRFit1176-6K1031176-6K1032026-10-22
04048223124581Tuohy II NRFit1176-6M1031176-6M1032026-10-22
04048223124611Tuohy II1170-6M1201170-6M1202026-10-22

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