VALLS1037

GUDID 10888551024952

VESSEL SEALING INSTRUMENT LIGASURE ATLAS HAND ACTIVATED

STERILMED, INC.

Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
Primary Device ID10888551024952
NIH Device Record Keyd02b0775-ba12-40dd-b893-795cfe5b5d8c
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberVALLS1037
Catalog NumberVALLS1037
Company DUNS175899459
Company NameSTERILMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com
Phone+1(888)541-0078
Emailcustomerservice@sterilmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110888551024952 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NUJELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10888551024952]

Ethylene Oxide


[10888551024952]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-22

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