GUDIDData
eudamed_udi Primary ID: 08711736951536

Postpartum kraamverband zelfkoelend, 1pc (UDI 08711736951536)

Manufactured by Changzhou Dailys Care Products Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Postpartum kraamverband zelfkoelend, 1pc - Primary ID 08711736951536

Device Regulatory Overview

The Postpartum kraamverband zelfkoelend, 1pc (Model/Catalog Number: C653) is a medical device manufactured by Changzhou Dailys Care Products Co.,Ltd. This product is indexed under FDA Product Code / Category Classification T04010299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
C653
Product Code / EMDN
T04010299
Device Name
Perineal Instant Cold Pack
Database Sync Date
2026-08-09 18:00:39

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 Postpartum kraamverband zelfkoelend, 1pc?

The registered manufacturer of record for Postpartum kraamverband zelfkoelend, 1pc is Changzhou Dailys Care Products Co.,Ltd.

What is the Primary UDI-DI identifier for Postpartum kraamverband zelfkoelend, 1pc?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08711736951536.

What classification code is assigned to this device?

This device is registered under product classification code T04010299.

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