eudamed_udi Primary ID: 05706069571882

HA CROS-FS TTGR (UDI 05706069571882)

Manufactured by WSAUD A/S

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The HA CROS-FS TTGR (Model/Catalog Number: 10971945) is a medical device manufactured by WSAUD A/S. This product is indexed under FDA Product Code / Category Classification Y214599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10971945
Product Code / EMDN: Y214599
Device Name: RIC
Database Sync Date: 2026-08-09 16:28:49

Full Regulatory Attributes

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{
    "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 HA CROS-FS TTGR?

The registered manufacturer of record for HA CROS-FS TTGR is WSAUD A/S.

What is the Primary UDI-DI identifier for HA CROS-FS TTGR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05706069571882.

What classification code is assigned to this device?

This device is registered under product classification code Y214599.

Similar Classification Devices (Y214599)

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