Nalgene™ Cryogenic Tube, 1.2 mL externally-threaded

GUDID 30850016058585

CRYOGENIC VIAL, PPCO; 1.2ML

Nalge Nunc International Corporation

General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium
Primary Device ID30850016058585
NIH Device Record Key648d6933-45fe-468a-913d-63add9c14a85
Commercial Distribution StatusIn Commercial Distribution
Brand NameNalgene™ Cryogenic Tube, 1.2 mL externally-threaded
Version Model Number5000-0012
Company DUNS080844844
Company NameNalge Nunc International Corporation
Device Count25
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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
GS110850016058581 [Primary]
GS130850016058585 [Package]
Contains: 10850016058581
Package: Case [500 Units]
In Commercial Distribution
GS180850016058580 [Unit of Use]

FDA Product Code

FMHCONTAINER, SPECIMEN, STERILE

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


[30850016058585]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-06-21
Device Publish Date2022-06-11

On-Brand Devices [Nalgene™ Cryogenic Tube, 1.2 mL externally-threaded]

30850016058585CRYOGENIC VIAL, PPCO; 1.2ML
30850016058684BLK STRL CRYOGNCVL PP; 1.2ML

Trademark Results [Nalgene]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NALGENE
NALGENE
73794489 1764075 Live/Registered
NALGE COMPANY
1989-04-20
NALGENE
NALGENE
72085893 0701346 Dead/Cancelled
NALGE COMPANY, INC.
1959-11-23

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