sup medic

GUDID 00850049592437

Supmedics Inc.

Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Primary Device ID00850049592437
NIH Device Record Keyfc8a2157-c776-408e-8378-e7f323d92ae4
Commercial Distribution StatusIn Commercial Distribution
Brand Namesup medic
Version Model NumberSKF01304
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 Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100850049592437 [Primary]

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 Date2025-05-23
Device Publish Date2025-05-15

Devices Manufactured by Supmedics Inc.

00810160181637 - supmedic2025-05-23
00810160181644 - supmedic2025-05-23
00810160181651 - supmedic2025-05-23
00810160181668 - supmedic2025-05-23
00850049592413 - supmedic2025-05-23
00850049592420 - supmedic2025-05-23
00850049592437 - sup medic2025-05-23
00850049592437 - sup medic2025-05-23
00850049592444 - supmedic2025-05-23

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