Batrik SAVEFACE Face Shield with Drape SF-8240

GUDID 00690521018952

SAVEFACE Face Shield with Drape

Batrik Medical Manufacturing Inc

Face splash shield, single-use
Primary Device ID00690521018952
NIH Device Record Keyada20ffb-e2b7-4b65-a81d-5c62a12eaaa0
Commercial Distribution StatusIn Commercial Distribution
Brand NameBatrik SAVEFACE Face Shield with Drape
Version Model NumberSF-8240
Catalog NumberSF-8240
Company DUNS243880700
Company NameBatrik Medical Manufacturing Inc
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com
Phone514-631-7988
Emailinfo@surgmed.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100690521018952 [Primary]

FDA Product Code

LYUAccessory, Surgical Apparel

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-02-04
Device Publish Date2022-01-27

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