GUDIDData
eudamed_udi Primary ID: 16953611800587

bocioland (UDI 16953611800587)

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 bocioland - Primary ID 16953611800587

Device Regulatory Overview

The bocioland (Model/Catalog Number: BL151) 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
BL151
Product Code / EMDN
T04010299
Device Name
Underpads
Database Sync Date
2026-08-09 18:47:19

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of bocioland?

The registered manufacturer of record for bocioland is Changzhou Dailys Care Products Co.,Ltd.

What is the Primary UDI-DI identifier for bocioland?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16953611800587.

What classification code is assigned to this device?

This device is registered under product classification code T04010299.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint