Lubri-soft Double J Ureteral Stent Two Ends Open, Blue 4.0 FR 30 CM (UDI 08681299261246)
Manufactured by DLR Medikal
Device Regulatory Overview
The Lubri-soft Double J Ureteral Stent Two Ends Open, Blue 4.0 FR 30 CM (Model/Catalog Number: 1604030) is a medical device manufactured by DLR Medikal. This product is indexed under FDA Product Code / Category Classification U020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1604030
- Product Code / EMDN
- U020302
- Device Name
- Lubri-soft Double J Ureteral Stent Two Ends Open, Blue 4.0 FR 30 CM
- Database Sync Date
- 2026-08-09 16:28:58
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 Lubri-soft Double J Ureteral Stent Two Ends Open, Blue 4.0 FR 30 CM?
The registered manufacturer of record for Lubri-soft Double J Ureteral Stent Two Ends Open, Blue 4.0 FR 30 CM is DLR Medikal.
What is the Primary UDI-DI identifier for Lubri-soft Double J Ureteral Stent Two Ends Open, Blue 4.0 FR 30 CM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681299261246.
What classification code is assigned to this device?
This device is registered under product classification code U020302.
Similar Classification Devices (U020302)
Other Devices by DLR Medikal
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