CUFF FIRST - NITRILE BLUE

GUDID 10860013366527

CUFF FIRST INC.

Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Primary Device ID10860013366527
NIH Device Record Key3273826b-2d06-4bee-8cfa-cf177aebc1e3
Commercial Distribution StatusIn Commercial Distribution
Brand NameCUFF FIRST - NITRILE BLUE
Version Model NumberCF003BN
Company DUNS119468310
Company NameCUFF FIRST INC.
Device Count125
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com
Phone(646)2963836
Emailmbs101@gmail.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860013366520 [Primary]
GS100860013366582 [Unit of Use]
GS110860013366527 [Package]
Contains: 00860013366520
Package: CASE [16 Units]
In Commercial Distribution

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 Date2025-04-02
Device Publish Date2025-03-25

On-Brand Devices [CUFF FIRST - NITRILE BLUE]

10860013366541CF004BN
10860013366534CF000BN
10860013366527CF003BN
10860013366510CF002BN
10860013366503CF001BN

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