LiNA McCartney Tube

GUDID 09349967002742

THE O R COMPANY PTY LTD

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Primary Device ID09349967002742
NIH Device Record Keyfb3da876-43e8-4471-b063-033f6112e66b
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiNA McCartney Tube
Version Model Number45-TV
Company DUNS744346235
Company NameTHE O R COMPANY PTY LTD
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter
Outer Diameter32 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS109349967002728 [Primary]
GS109349967002735 [Package]
Contains: 09349967002728
Package: Outer [5 Units]
In Commercial Distribution
GS109349967002742 [Package]
Contains: 09349967002735
Package: Shipper [3 Units]
In Commercial Distribution

FDA Product Code

HEWCuldoscope (And Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-04-04
Device Publish Date2019-03-27

On-Brand Devices [LiNA McCartney Tube]

0934996700274245-TV
0934996700271135-TV

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