TLS, Quintube (UDI 6630)
Manufactured by Stryker Leibinger GmbH & Co. KG
Device Regulatory Overview
The TLS, Quintube (Model/Catalog Number: 6630) is a medical device manufactured by Stryker Leibinger GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification GCY within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 6630
- Product Code / EMDN
- GCY
- Device Name
- QUINTUBE Monitor Pk (5tubes/pk,24pk/cs)
- Database Sync Date
- 2026-08-09 09:16:48
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of TLS, Quintube?
The registered manufacturer of record for TLS, Quintube is Stryker Leibinger GmbH & Co. KG.
What is the Primary UDI-DI identifier for TLS, Quintube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6630.
What classification code is assigned to this device?
This device is registered under product classification code GCY.
Similar Classification Devices (GCY)
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