COPAL® knee moulds 5159869

GUDID 04260102139275

COPAL® knee moulds are sterile single-use moulds used for the preparation of spacers that are intended as temporary knee replacements as part of two-stage septic joint prosthesis revision. COPAL® knee moulds comprise a tibial component and a femoral component, which together form a bearing and move against one another. They can be used in both the right and the left knee joint. The spacer function provides that after removal of the prosthesis the existing joint space is retained and contraction of the musculature and the surrounding tissues is prevented. COPAL® knee moulds are intended for single use and must not be re-used or resterilised.

Heraeus Medical GmbH

Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould Orthopaedic cement spacer mould
Primary Device ID04260102139275
NIH Device Record Keye163e144-f300-4368-b872-2b50dac05f29
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOPAL® knee moulds
Version Model NumberM
Catalog Number5159869
Company DUNS333623937
Company NameHeraeus Medical GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104260102139268 [Primary]
GS104260102139275 [Package]
Contains: 04260102139268
Package: Carton [1 Units]
In Commercial Distribution
GS104260102139282 [Package]
Package: Pallet [64 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-01
Device Publish Date2023-04-21

On-Brand Devices [COPAL® knee moulds]

04260102139299COPAL® knee moulds are sterile single-use moulds used for the preparation of spacers that are i
04260102139275COPAL® knee moulds are sterile single-use moulds used for the preparation of spacers that are i
04260102139244COPAL® knee moulds are sterile single-use moulds used for the preparation of spacers that are i

Trademark Results [COPAL]

Mark Image

Registration | Serial
Company
Trademark
Application Date
COPAL
COPAL
97715895 not registered Live/Pending
In Mocean Group LLC
2022-12-13
COPAL
COPAL
79225667 5663402 Live/Registered
Krzysztof Bawol
2017-08-21
COPAL
COPAL
79131038 4473176 Live/Registered
NIDEC COPAL CORPORATION
2013-04-15
COPAL
COPAL
77913448 3834767 Dead/Cancelled
Thiem, Hannah L
2010-01-16
COPAL
COPAL
77882561 not registered Dead/Abandoned
Chokron, Melanie
2009-11-30
COPAL
COPAL
77655389 not registered Dead/Abandoned
Chokron, Melanie
2009-01-23
COPAL
COPAL
76712615 4445460 Live/Registered
Heraeus Medical GmbH
2012-10-12
COPAL
COPAL
76628054 3134732 Dead/Cancelled
Heraeus Kulzer GmbH
2005-01-18
COPAL
COPAL
75642936 not registered Dead/Abandoned
Maruba Therapy, Inc.
1999-02-16
COPAL
COPAL
75416593 2228206 Dead/Cancelled
Merck KGaA, Kommanditgesellschaft auf Aktien
1998-01-12
COPAL
COPAL
75196772 not registered Dead/Abandoned
Maruba Therapy, Inc.
1996-11-12
COPAL
COPAL
74548595 1982985 Live/Registered
ADOBE INC.
1994-07-05

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.