STERILIZATION TUBING

GUDID D89260705600451

MAXILL, INC.

Sterilization packaging, single-use
Primary Device IDD89260705600451
NIH Device Record Keyb3f949e4-d0d3-48a9-b320-386c519d59a6
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTERILIZATION TUBING
Version Model Number6070560045
Company DUNS079343581
Company NameMAXILL, INC.
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD89260705600450 [Primary]
HIBCCD89260705600451 [Package]
Contains: D89260705600450
Package: Case [98 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRGWrap, Sterilization

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-27
Device Publish Date2022-09-19

On-Brand Devices [STERILIZATION TUBING]

D892607056004716070560047
D892607056004616070560046
D892607056004516070560045

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