Catheter Mount Tubing; with right angled swivel connector with bronchoscope/suct

GUDID 24250105628795

n.a.

VBM Medizintechnik GmbH

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• Primary Device ID: 24250105628795
• NIH Device Record Key: 9adeafc3-29c8-4610-891e-048b27f1e672
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Catheter Mount Tubing; with right angled swivel connector with bronchoscope/suct
• Version Model Number: 65-50-130
• Company DUNS: 324869601
• Company Name: VBM Medizintechnik GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de
• Phone: +49745495960
• Email: info@vbm-medical.de

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat
• Special Storage Condition, Specify: Between 0 and 0 *keep dry, keep away from sunlight and heat

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250105602173 [Previous]
GS1	14250105628798 [Primary]
GS1	24250105628795 [Package]; Contains: 14250105628798; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• BZO: Set, Tubing And Support, Ventilator (W Harness)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-11-22
• Device Publish Date: 2020-09-18

On-Brand Devices [Catheter Mount Tubing; with right angled swivel connector with bronchoscope/suct]

• 24250105628795: n.a.
• 14250105602439: n.a.