GUDIDData
eudamed_udi Primary ID: 04260018193897

babylove Traubenkern-Kissen 12x12 cm (UDI 04260018193897)

Manufactured by GRÜNSPECHT Naturprodukte GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for babylove Traubenkern-Kissen 12x12 cm - Primary ID 04260018193897

Device Regulatory Overview

The babylove Traubenkern-Kissen 12x12 cm (Model/Catalog Number: DM152-V3) is a medical device manufactured by GRÜNSPECHT Naturprodukte GmbH. This product is indexed under FDA Product Code / Category Classification M9001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DM152-V3
Product Code / EMDN
M9001
Device Name
Produkte mit Naturfüllstoffen zur Wärmetherapie
Database Sync Date
2026-08-09 18:53:39

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 babylove Traubenkern-Kissen 12x12 cm?

The registered manufacturer of record for babylove Traubenkern-Kissen 12x12 cm is GRÜNSPECHT Naturprodukte GmbH.

What is the Primary UDI-DI identifier for babylove Traubenkern-Kissen 12x12 cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260018193897.

What classification code is assigned to this device?

This device is registered under product classification code M9001.

Programmatic Export

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

JSON API Endpoint