GUDIDData
gudid Primary ID: PSF08LT

PhotonSaber F (UDI PSF08LT)

Manufactured by STRYKER CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PhotonSaber F - Primary ID PSF08LT

Device Regulatory Overview

The PhotonSaber F (Model/Catalog Number: PSF08LT) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification JOL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PSF08LT
Product Code / EMDN
JOL
Device Name
F Aspirator, 8 Fr, Long, Teardrop
Database Sync Date
2026-08-09 09:31:28

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 PhotonSaber F?

The registered manufacturer of record for PhotonSaber F is STRYKER CORPORATION.

What is the Primary UDI-DI identifier for PhotonSaber F?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PSF08LT.

What classification code is assigned to this device?

This device is registered under product classification code JOL.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint