PullUp Probe Cover Kit 2211

GUDID 10841912105653

PROTEK MEDICAL PRODUCTS, INC.

Cable/lead/sensor/probe cover, sterile
Primary Device ID10841912105653
NIH Device Record Keyc05db419-e692-4758-91f5-01dcfda4aead
Commercial Distribution StatusIn Commercial Distribution
Brand NamePullUp Probe Cover Kit
Version Model Number2211
Catalog Number2211
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100841912105656 [Primary]
GS110841912105653 [Package]
Contains: 00841912105656
Package: [24 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KKXDrape, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-08-13
Device Publish Date2018-07-13

On-Brand Devices [PullUp Probe Cover Kit]

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008419121044752097
108419121043591512
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108419121006271096
108419121003822233
108419121003752233
108419121003682231
108419121002072099
008419121001942099
008419121001872097
108419121001772097
008419121001632097
108419121001532096
008419121001492095
108419121067352048
108419121063152044

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