Quicktrach II

GUDID 14250105629979

VBM Medizintechnik GmbH

Cricothyrotomy kit, single-use
Primary Device ID14250105629979
NIH Device Record Key7073d282-78f9-4c23-811a-312b5ba8fd41
Commercial Distribution StatusIn Commercial Distribution
Brand NameQuicktrach II
Version Model Number30-10-004-1
Company DUNS324869601
Company NameVBM Medizintechnik GmbH
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 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+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de
Phone+49745495960
Emailinfo@vbm-medical.de

Device Dimensions

Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter
Lumen/Inner Diameter4 Millimeter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry, Keep away from sunlight and heat

Device Identifiers

Device Issuing AgencyDevice ID
GS104250105604993 [Previous]
GS104250105629972 [Primary]
GS114250105629979 [Package]
Contains: 04250105629972
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BTOTube, Tracheostomy (W/Wo Connector)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-16
Device Publish Date2023-11-08

On-Brand Devices [Quicktrach II ]

2425010562998330-10-904-1
1425010562997930-10-004-1
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.