eudamed_udi Primary ID: 06974567461618

emergency blanket (UDI 06974567461618)

Manufactured by Danyang Sunmed Healthcare Corporation

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

Scannable UDI-DI Representation

Device Regulatory Overview

The emergency blanket (Model/Catalog Number: 160*210cm) is a medical device manufactured by Danyang Sunmed Healthcare Corporation. This product is indexed under FDA Product Code / Category Classification T0299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 160*210cm
Product Code / EMDN: T0299
Device Name: Rescue sheet
Database Sync Date: 2026-08-09 16:51:57

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 emergency blanket?

The registered manufacturer of record for emergency blanket is Danyang Sunmed Healthcare Corporation.

What is the Primary UDI-DI identifier for emergency blanket?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974567461618.

What classification code is assigned to this device?

This device is registered under product classification code T0299.

Similar Classification Devices (T0299)

Other Devices by Danyang Sunmed Healthcare Corporation

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