Tobey micro antrum punch 30-305-00

GUDID 04250381813362

backwards cutting, rotatable, shaft curved downwards, irrig. channel, 10 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, alligator, reusable
Primary Device ID04250381813362
NIH Device Record Key64ccad1c-a976-4770-960e-ac13219d7a6e
Commercial Distribution StatusIn Commercial Distribution
Brand NameTobey micro antrum punch
Version Model Number30-305-00
Catalog Number30-305-00
Company DUNS332893028
Company NameSpiggle & Theis Medizintechnik GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com
Phone+492206908165
Emailc.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250381813362 [Primary]

FDA Product Code

LRCINSTRUMENT, ENT MANUAL SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


[04250381813362]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-19
Device Publish Date2023-06-09

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