n/a

GUDID 04250105609660

Hand inflator

VBM Medizintechnik GmbH

Surgical pneumatic tourniquet system

• Primary Device ID: 04250105609660
• NIH Device Record Key: eba6b8aa-8d97-4464-860e-4dd5dc3cd7fe
• Commercial Distribution Discontinuation: 2025-04-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: n/a
• Version Model Number: 20-10-333
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250105609660 [Primary]

FDA Product Code

• KCY: Tourniquet, Pneumatic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2025-04-16
• Device Publish Date: 2019-10-08

On-Brand Devices [n/a]

• 04250105615456: Manujet III
• 04250105612455: Quicktrach II Emergency Cricothyrotomy Set for adult
• 04250105608595: Manujet III including Jet-Ventilations Catheters
• 04250105605136: Jet-Ventilation Catheter for infant
• 04250105605129: Jet-Ventilation Catheter for child
• 04250105605112: Jet-Ventilation Catheter for adult
• 14250105605102: Jet-Ventilation Catheter for infant
• 14250105605096: Jet-Ventilation Catheter for child
• 14250105605089: Jet-Ventilation Catheter for adult
• 04250105604993: Quicktrach II Emergency Cricothyrotomy Set for adult
• 04250105604290: Connecting Tube for Cuff Pressure Control
• 14250105604280: Connecting Tube for Manujet III
• 04250105605723: PEDIATRIC Cuff Pressure Gauge with hook
• 04250105600483: POCKET Cuff Pressure Gauge with hook
• 04250105600476: SENSITIVE Cuff Pressure Gauge with hook
• 04250105600469: SENSITIVE Cuff Pressure Gauge without hook
• 14250105613459: Single Cuff disposable for super long leg, contour shape
• 04250105609660: Hand inflator