Bone drill DCC114021

GUDID 04250337105114

joimax® Bone Drill, 4.0 mm, cannulated, sterile

Joimax GmbH

Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use Bone-resection orthopaedic reamer, single-use
Primary Device ID04250337105114
NIH Device Record Key362a6ee8-585f-4f1a-a561-4ccbf1ad7876
Commercial Distribution StatusIn Commercial Distribution
Brand NameBone drill
Version Model NumberDCC114021
Catalog NumberDCC114021
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
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
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

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Device Identifiers

Device Issuing AgencyDevice ID
GS104250337105114 [Primary]

FDA Product Code

HTOREAMER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-09-13
Device Publish Date2022-12-30

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