GUDIDData
eudamed_udi Primary ID: 07331427091191

Sanicare nattdräkt, k.b. knäppning hö. axel, XXS/130 (UDI 07331427091191)

Manufactured by Swereco AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sanicare nattdräkt, k.b. knäppning hö. axel, XXS/130 - Primary ID 07331427091191

Device Regulatory Overview

The Sanicare nattdräkt, k.b. knäppning hö. axel, XXS/130 (Model/Catalog Number: 6099) is a medical device manufactured by Swereco AB. This product is indexed under FDA Product Code / Category Classification T0499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6099
Product Code / EMDN
T0499
Device Name
Nightwear
Database Sync Date
2026-08-09 16:45:59

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 Sanicare nattdräkt, k.b. knäppning hö. axel, XXS/130?

The registered manufacturer of record for Sanicare nattdräkt, k.b. knäppning hö. axel, XXS/130 is Swereco AB.

What is the Primary UDI-DI identifier for Sanicare nattdräkt, k.b. knäppning hö. axel, XXS/130?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07331427091191.

What classification code is assigned to this device?

This device is registered under product classification code T0499.

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