Inserter for plastic vent tubes with 10-759-00

GUDID 04250676733436

one each mandrin for 1.00 mm and 1.2 mm diameter

Spiggle & Theis Medizintechnik GmbH

Tympanostomy tube inserter, reusable
Primary Device ID04250676733436
NIH Device Record Keye3829ce4-e1e9-4cc5-b2c0-1b81eea2dda7
Commercial Distribution StatusIn Commercial Distribution
Brand NameInserter for plastic vent tubes with
Version Model Number10-759-00
Catalog Number10-759-00
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
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
GS104250676733436 [Primary]

FDA Product Code

LRCINSTRUMENT, ENT MANUAL SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


[04250676733436]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-20
Device Publish Date2023-07-12

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