Shaft obturator BSHO04175

GUDID 04250337120346

Shaft obturator for endoscope shaft

Joimax GmbH

Rigid endoscope obturator
Primary Device ID04250337120346
NIH Device Record Keyf2650c57-dea4-413e-a70c-19cf32910493
Commercial Distribution StatusIn Commercial Distribution
Brand NameShaft obturator
Version Model NumberBSHO04175
Catalog NumberBSHO04175
Company DUNS344267187
Company NameJoimax 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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104250337120346 [Primary]

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

[04250337120346]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-09
Device Publish Date2023-09-29

Devices Manufactured by Joimax GmbH

04250337101741 - iLESSYS®2024-09-11 TESSYS® Steel Ruler
04250337102854 - Adapter2024-07-15 Lightsource Adaptor for Foraminoscope (Wolf)
04250337102861 - Adapter2024-07-15 Lightsource Adaptor for Foraminoscope (Storz)
04250337100737 - Flatscreen2024-05-03 joimax® Flatscreen Monitor 19.0'' TFT
04250337100744 - trolley2024-05-03 joimax® Monitor Trolley, grey
04250337105473 - Flatscreen2024-05-03 Flatscreen Monitor 24.0'' TFT
04250337106340 - Flatscreen2024-05-03 joimax® Flatscreen Monitor 42.0'' TFT
04250337109396 - Flatscreen2024-05-03 joimax® Flatscreen Monitor 24.0'' TFT
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.