CESSYS® TNC582820Y

GUDID 04250337116837

CESSYS® Dorsal DIN-Norm-Container, yellow Lid

Joimax GmbH

Device sterilization/disinfection container, reusable
Primary Device ID04250337116837
NIH Device Record Keyd8b24a90-583e-41e3-b690-9dda5cb7e9c0
Commercial Distribution StatusIn Commercial Distribution
Brand NameCESSYS®
Version Model NumberTNC582820Y
Catalog NumberTNC582820Y
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

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 Identifiers

Device Issuing AgencyDevice ID
GS104250337116837 [Primary]

FDA Product Code

FSMTRAY, SURGICAL, INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


[04250337116837]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-04-04
Device Publish Date2022-12-30

On-Brand Devices [CESSYS®]

04250337114697CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo
04250337114680CESSYS® Dorsal FHD Laminoscope (4.7 WCh), ocular
04250337105879CESSYS® Cervical Hybrid Scope, combo
04250337116837CESSYS® Dorsal DIN-Norm-Container, yellow Lid
04250337108818CESSYS® DIN-Norm-Container, gold Lid
04250337105152CESSYS® Cervical Reamer

Trademark Results [CESSYS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CESSYS
CESSYS
79062669 3799655 Live/Registered
joimax GmbH
2008-10-10

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