TUNNELER

GUDID 50884908005375

TESIO® BLUNT TUNNELER

Medical Components, Inc.

Vascular graft tunneller
Primary Device ID50884908005375
NIH Device Record Keyfcb0c640-098e-4f2d-8086-ff29bc0aa885
Commercial Distribution StatusIn Commercial Distribution
Brand NameTUNNELER
Version Model NumberBTT
Company DUNS038000253
Company NameMedical Components, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com
Phone+1(215)256-4201
Emailclinical@medcompnet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100884908005370 [Primary]
GS150884908005375 [Package]
Contains: 00884908005370
Package: box [5 Units]
In Commercial Distribution

FDA Product Code

MZYGraft,vascular,stainless steel tunneler

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-09-03
Device Publish Date2016-10-21

On-Brand Devices [TUNNELER]

508849080311142- BARBED TUNNELERS FOR 6F PRO-LINE®
50884908005375TESIO® BLUNT TUNNELER

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