GUDIDData
eudamed_udi Primary ID: 00810170556203

PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs (UDI 00810170556203)

Manufactured by SLMP LLC d.b.a. StatLab Medical Products

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs - Primary ID 00810170556203

Device Regulatory Overview

The PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs (Model/Catalog Number: DL601TN) is a medical device manufactured by SLMP LLC d.b.a. StatLab Medical Products. This product is indexed under FDA Product Code / Category Classification W0202050385 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DL601TN
Product Code / EMDN
W0202050385
Device Name
PathFlow PiSmart Cassettes
Database Sync Date
2026-08-09 16:45:56

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs?

The registered manufacturer of record for PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs is SLMP LLC d.b.a. StatLab Medical Products.

What is the Primary UDI-DI identifier for PathFlow PiSmart Laser Cassette, Rear Hinge, Lid Separate, Slotted, Threaded, Tan, 2000/cs?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810170556203.

What classification code is assigned to this device?

This device is registered under product classification code W0202050385.

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