GUDIDData
eudamed_udi Primary ID: 20884838115006

NEONATAL SOFT SINGLE-PATIENT CUFF SIZE#4 (UDI 20884838115006)

Manufactured by Philips Medizin Systeme Böblingen GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEONATAL SOFT SINGLE-PATIENT CUFF SIZE#4 - Primary ID 20884838115006

Device Regulatory Overview

The NEONATAL SOFT SINGLE-PATIENT CUFF SIZE#4 (Model/Catalog Number: M1872S) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z1203020285 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M1872S
Product Code / EMDN
Z1203020285
Device Name
Neonatal Single & Soft-Single NIBP Cuffs
Database Sync Date
2026-08-09 16:48:02

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 NEONATAL SOFT SINGLE-PATIENT CUFF SIZE#4?

The registered manufacturer of record for NEONATAL SOFT SINGLE-PATIENT CUFF SIZE#4 is Philips Medizin Systeme Böblingen GmbH.

What is the Primary UDI-DI identifier for NEONATAL SOFT SINGLE-PATIENT CUFF SIZE#4?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20884838115006.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020285.

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