Curette DEC155011

GUDID 04250337120537

Curette

Joimax GmbH

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable
Primary Device ID04250337120537
NIH Device Record Keyadf56527-1555-495a-9073-863caf16510f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCurette
Version Model NumberDEC155011
Catalog NumberDEC155011
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

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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
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Device Size Text, specify0
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Device Identifiers

Device Issuing AgencyDevice ID
GS104250337120537 [Primary]

FDA Product Code

FZSCurette, Surgical, General Use

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

Moist Heat or Steam Sterilization


[04250337120537]

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

On-Brand Devices [Curette]

04250337120544Curette
04250337120537Curette

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