Uline Wht 3 Mil Nitrile Glvs-L

GUDID 30850015055189

ULINE, INC.

Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Primary Device ID30850015055189
NIH Device Record Key44c283f4-57d1-45e7-9b9b-81e135dc9218
Commercial Distribution StatusIn Commercial Distribution
Brand NameUline Wht 3 Mil Nitrile Glvs-L
Version Model NumberS-21082-L
Company DUNS039612668
Company NameULINE, INC.
Device Count200
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 Batchfalse
Serial Numberfalse
Manufacturing Datefalse
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
GS100850015055225 [Unit of Use]
GS110850015055222 [Primary]
GS130850015055189 [Package]
Contains: 10850015055222
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LZAPolymer Patient Examination Glove

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-08-05
Device Publish Date2021-07-28

Devices Manufactured by ULINE, INC.

30850015055509 - ULINE REUSABLE EARPLUGS - UNCORDED2024-08-02
30850015055516 - ULINE REUSABLE EARPLUGS - CORDED2024-08-02
30850015055523 - ULINE BULLET EARPLUGS - UNCORDED2024-07-31
30850015055530 - ULINE BULLET EARPLUGS - CORDED2024-07-31
30850015055547 - ULINE BELL EARPLUGS - UNCORDED2024-07-31
30850015055554 - ULINE BELL EARPLUGS - CORDED2024-07-31
30850015055493 - ULINE BULLET EARPLUGS REFILL2024-05-21
00850015055713 - ULINE EARPLUGS IN A BUCKET2024-05-21
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.