OPMI® Drapes sterile

GUDID 04049539102218

Carl Zeiss Meditec AG

Instrument/equipment drape, single-use, sterile
Primary Device ID04049539102218
NIH Device Record Keyb0aed675-909a-421c-a05f-85833a6a801e
Commercial Distribution StatusIn Commercial Distribution
Brand NameOPMI® Drapes sterile
Version Model Number306071-0000-000
Company DUNS342228620
Company NameCarl Zeiss Meditec AG
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Height118 Inch
Width48 Inch
Height300 Centimeter
Width122 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104049539101211 [Primary]
GS104049539102003 [Package]
Contains: 04049539101211
Package: [5 Units]
In Commercial Distribution
GS104049539102218 [Package]
Contains: 04049539102003
Package: [10 Units]
In Commercial Distribution

FDA Product Code

KKXDrape, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-08-15

On-Brand Devices [OPMI® Drapes sterile]

04049539102294326082-0000-000
04049539101280326018-0000-000
04049539101273326013-0000-000
04049539101266326009-0000-000
04049539102256326005-0000-000
04049539101242306079-0000-000
04049539101235306075-0000-000
04049539102225306073-0000-000
04049539102218306071-0000-000
04049539102201306070-0000-000
04049539102195306026-0000-000
04049539101181306025-0000-000

Trademark Results [OPMI]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OPMI
OPMI
73267838 1173004 Live/Registered
Carl-Zeiss-Stiftung
1980-06-25

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