SUPMEDIC

GUDID 00810160180289

Supmedics Inc.

Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Primary Device ID00810160180289
NIH Device Record Key64e03d48-fdda-4d77-b170-cc641d8cc9b0
Commercial Distribution StatusIn Commercial Distribution
Brand NameSUPMEDIC
Version Model NumberSKF02302
Company DUNS107150886
Company NameSupmedics 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 Numbertrue
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
GS100810160180289 [Primary]

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 Date2024-11-12
Device Publish Date2024-11-04

On-Brand Devices [SUPMEDIC]

00810160180395SKF03301
00810160180388SKF03304
00810160180371SKF03303
00810160180364SKF03302
00810160180357SKF3301
00810160180340SKF3304
00810160180333SKF3303
00810160180326SKF3302
00810160180319SKF02305
00810160180302SKF02304
00810160180296SKF02303
00810160180289SKF02302
00810160180272SKF2305
00810160180265SKF2304
00810160180258SKF2303
00810160180241SKF2302

Trademark Results [SUPMEDIC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SUPMEDIC
SUPMEDIC
97275035 not registered Live/Pending
Supmedics Inc.
2022-02-18

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