Wellstar Gyn Lap

GUDID 00817395021967

Wellstar Gyn Lap

PACKROOM LLC

Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use
Primary Device ID00817395021967
NIH Device Record Keyefb2e171-63ce-4e75-90ae-612aa4371e7b
Commercial Distribution StatusIn Commercial Distribution
Brand NameWellstar Gyn Lap
Version Model NumberWS280
Company DUNS015179820
Company NamePACKROOM LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100817395021967 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-21
Device Publish Date2020-10-13

On-Brand Devices [Wellstar Gyn Lap ]

00817395021967Wellstar Gyn Lap
00817395023558Wellstar Gyn Lap

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.