ParaProTM XLT (UDI 00860008410436)
Manufactured by SLMP LLC d.b.a. StatLab Medical Products
Device Regulatory Overview
The ParaProTM XLT (Model/Catalog Number: PPXLT) is a medical device manufactured by SLMP LLC d.b.a. StatLab Medical Products. This product is indexed under FDA Product Code / Category Classification W05030599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PPXLT
- Product Code / EMDN
- W05030599
- Device Name
- ParaProTM SEM
- Database Sync Date
- 2026-08-09 16:30:35
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ParaProTM XLT?
The registered manufacturer of record for ParaProTM XLT is SLMP LLC d.b.a. StatLab Medical Products.
What is the Primary UDI-DI identifier for ParaProTM XLT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00860008410436.
What classification code is assigned to this device?
This device is registered under product classification code W05030599.
Similar Classification Devices (W05030599)
Other Devices by SLMP LLC d.b.a. StatLab Medical Products
- → PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Biopsy, Threaded, Blue, 2000/cs
- → PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Biopsy, Threaded, Peach, 2000/cs
- → PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs
- → PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Biopsy, Threaded, Orange, 2000/cs
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint