Indian Knife IK150610

GUDID 04250337120476

Indian Knife with handle

Joimax GmbH

Bone lever/elevator, reusable
Primary Device ID04250337120476
NIH Device Record Key39fb0862-39c1-48a6-aad6-4f5e5679e6d9
Commercial Distribution StatusIn Commercial Distribution
Brand NameIndian Knife
Version Model NumberIK150610
Catalog NumberIK150610
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
GS104250337120476 [Primary]

FDA Product Code

FZSCurette, Surgical, General Use

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

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

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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
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