CoForm 604037

GUDID 17310236040375

Directa AB

Dental mould Dental mould Dental mould Dental mould
Primary Device ID17310236040375
NIH Device Record Keya0d78462-a695-45ec-ab60-f84304940c68
Commercial Distribution StatusIn Commercial Distribution
Brand NameCoForm
Version Model Number11 Distal
Catalog Number604037
Company DUNS353954381
Company NameDirecta AB
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS117310236040375 [Primary]

FDA Product Code

ELZCrown, Preformed

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-15
Device Publish Date2022-12-07

On-Brand Devices [CoForm]

1731023604051141-42 Distal
1731023604050441-42 Mesial
1731023604049831-32 Distal
1731023604048131-32 Mesial
1731023604047423 Distal
1731023604046723 Mesial
1731023604045013 Distal
1731023604044313 Mesial
1731023604043622 Distal
1731023604042922 Mesial
1731023604041212 Distal
1731023604040512 Mesial
1731023604039921 Distal
1731023604038221 Mesial
1731023604037511 Distal
1731023604036811 Mesial
17310236040351Assortment A
17310236040344Assortment B

Trademark Results [CoForm]

Mark Image

Registration | Serial
Company
Trademark
Application Date
COFORM
COFORM
85610716 not registered Dead/Abandoned
ENCAP Technologies, LLC
2012-04-27
COFORM
COFORM
85424497 4238958 Dead/Cancelled
Ansell Limited
2011-09-16
COFORM
COFORM
79382727 not registered Live/Pending
Directa AB
2023-10-11
COFORM
COFORM
72374796 0939722 Dead/Cancelled
CONTINENTAL SCREW COMPANY
1970-10-30

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