Monopolar Forceps 50-400-23

GUDID 04250381858882

Monopolar coagulation forceps, rotatable, serrated, straight, smoke evacuation, shaft 3.0 mm, 23.5 cm

Spiggle & Theis Medizintechnik GmbH

Endoscopic electrosurgical electrode, monopolar, reusable
Primary Device ID04250381858882
NIH Device Record Keye4b48271-fcda-4ac9-a8de-bf9ee5ce2f1e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMonopolar Forceps
Version Model Number50-400-23
Catalog Number50-400-23
Company DUNS332893028
Company NameSpiggle & Theis Medizintechnik GmbH
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+492206908153
Emailp.stockmann@spiggle-theis.com

Device Dimensions

Length23.5 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104250381858882 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250381858882]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-06-17
Device Publish Date2019-06-07

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