Instrument Cover 1238

GUDID 00841912104567

PROTEK MEDICAL PRODUCTS, INC.

Instrument/equipment drape, single-use, sterile
Primary Device ID00841912104567
NIH Device Record Key90c7afa5-b854-42c5-bcc9-bd6e580ef2f9
Commercial Distribution StatusIn Commercial Distribution
Brand NameInstrument Cover
Version Model Number1238
Catalog Number1238
Company DUNS965417181
Company NamePROTEK MEDICAL PRODUCTS, 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100841912104567 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MMPCover, Barrier, Protective

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-23

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