GUDIDData
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eudamed_udi Primary ID: 08058481763732

TELO SCHIENALE IN NYLON IMBOTTITO PER CARROZZINA PMN ACTIVA 51 (UDI 08058481763732)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TELO SCHIENALE IN NYLON IMBOTTITO PER CARROZZINA PMN ACTIVA 51 - Primary ID 08058481763732

Device Regulatory Overview

The TELO SCHIENALE IN NYLON IMBOTTITO PER CARROZZINA PMN ACTIVA 51 (Model/Catalog Number: PX17R100) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification Y122499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX17R100
Product Code / EMDN
Y122499
Device Name
RICAMBI CARROZZINE LEGGERE
Database Sync Date
2026-08-09 16:59:11

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 TELO SCHIENALE IN NYLON IMBOTTITO PER CARROZZINA PMN ACTIVA 51?

The registered manufacturer of record for TELO SCHIENALE IN NYLON IMBOTTITO PER CARROZZINA PMN ACTIVA 51 is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for TELO SCHIENALE IN NYLON IMBOTTITO PER CARROZZINA PMN ACTIVA 51?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481763732.

What classification code is assigned to this device?

This device is registered under product classification code Y122499.

Similar Classification Devices (Y122499)

Other Devices by PRAXIS MEDICAL NETWORK SRL

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