eudamed_udi
Primary ID: 08681299261918
Lubri-soft Double J Ureteral Stent 6.5 FR 26 CM (UDI 08681299261918)
Manufactured by DLR Medikal
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lubri-soft Double J Ureteral Stent 6.5 FR 26 CM - Primary ID 08681299261918
Device Regulatory Overview
The Lubri-soft Double J Ureteral Stent 6.5 FR 26 CM (Model/Catalog Number: 1606526) 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
- 1606526
- Product Code / EMDN
- U020302
- Device Name
- Lubri-soft Double J Ureteral Stent 6.5 FR 26 CM
- Database Sync Date
- 2026-08-09 16:29:47
Full Regulatory Attributes
🔒 Token Gated
{
"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 6.5 FR 26 CM?
The registered manufacturer of record for Lubri-soft Double J Ureteral Stent 6.5 FR 26 CM is DLR Medikal.
What is the Primary UDI-DI identifier for Lubri-soft Double J Ureteral Stent 6.5 FR 26 CM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681299261918.
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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