+++++House suction cannula, Luer-Lock 10-308-15

GUDID 04250381801925

7 cm, 1.5 mm

Spiggle & Theis Medizintechnik GmbH

ENT suction dissector
Primary Device ID04250381801925
NIH Device Record Keyfde65106-c16f-4f7f-bb70-8e074212b7f2
Commercial Distribution StatusIn Commercial Distribution
Brand Name+++++House suction cannula, Luer-Lock
Version Model Number10-308-15
Catalog Number10-308-15
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
GS104250381801925 [Primary]

FDA Product Code

JZFTUBE, EAR SUCTION

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

Moist Heat or Steam Sterilization


[04250381801925]

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

On-Brand Devices [+++++House suction cannula, Luer-Lock]

042503818565366 cm, 1.0 mm
042503818565296 cm, 0.8 mm
042503818019637 cm, 2.5 mm
042503818019567 cm, 2.2 mm
042503818019257 cm, 1.5 mm
042503818018957 cm, 0.8 mm
042503818018887 cm, 0.6 mm

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.