Probe Cover Kit 1026

GUDID 10841912100573

PROTEK MEDICAL PRODUCTS, INC.

Cable/lead/sensor/probe cover, sterile
Primary Device ID10841912100573
NIH Device Record Key989d6790-9466-4198-b68c-db8dcdbe0acd
Commercial Distribution StatusIn Commercial Distribution
Brand NameProbe Cover Kit
Version Model Number1026
Catalog Number1026
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
GS100841912100576 [Primary]
GS110841912100573 [Package]
Contains: 00841912100576
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 StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-16

On-Brand Devices [Probe Cover Kit ]

108419121056771467
008419121049492221
008419121045741241
108419121042742320
108419121007571460
108419121007401460
108419121007331460
108419121007261460
108419121007191270
108419121007021240
108419121006961236
108419121005731026
108419121004742450
108419121004672450
108419121004502320
108419121004432320
108419121004362290
108419121004292270
108419121004122252
108419121004052250
108419121003992236
108419121003512230
108419121003202220
008419121003162219
008419121003092216
008419121002932220
108419121002522210
108419121002452208

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.