House suction cannula, Luer-Lock 10-308-10

GUDID 04250381801901

7 cm, 1.0 mm

Spiggle & Theis Medizintechnik GmbH

Surgical irrigation/aspiration cannula, non-illuminating, reusable
Primary Device ID04250381801901
NIH Device Record Key7694a4bc-ce0d-4c93-b8d5-c368d51825e0
Commercial Distribution StatusIn Commercial Distribution
Brand NameHouse suction cannula, Luer-Lock
Version Model Number10-308-10
Catalog Number10-308-10
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104250381801901 [Primary]

FDA Product Code

JZFTUBE, EAR SUCTION

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


[04250381801901]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-15
Device Publish Date2023-06-07

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04250676725561 - Kerrison sphenoid punch2024-11-19 90° upw., golden tip, totally detachable 1 mm, 23 cm
04250676725974 - Kerrison sphenoid punch2024-11-19 40° upw., golden tip, totally detachable 1 mm, 20 cm

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