Prestige Ameritech

GUDID 00852212003276

Fluid Resistant Surgical Tie Mask, High Filtration

PRESTIGE AMERITECH, LTD.

Surgical/medical face mask, single-use
Primary Device ID00852212003276
NIH Device Record Key418a98ce-aa60-4e53-8ab9-898cf9f3572d
Commercial Distribution StatusIn Commercial Distribution
Brand NamePrestige Ameritech
Version Model Number200601-04
Company DUNS199692794
Company NamePRESTIGE AMERITECH, LTD.
Device Count50
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18664018972
Emailorders@prestigeam.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100852212003276 [Primary]
GS110852212003273 [Package]
Package: Case [6 Units]
In Commercial Distribution
GS180852212003272 [Unit of Use]

FDA Product Code

FXXMask, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-05-06
Device Publish Date2016-09-26

On-Brand Devices [Prestige Ameritech]

00852212003276Fluid Resistant Surgical Tie Mask, High Filtration
10852212003259Fluid Resistant Earloop Mask, High Filtration

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