GUDIDData
eudamed_udi Primary ID: 04640003830455

Spirometer SMP 21/01 RD (UDI 04640003830455)

Manufactured by Research and Production Company «Monitor» Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spirometer SMP 21/01 RD - Primary ID 04640003830455

Device Regulatory Overview

The Spirometer SMP 21/01 RD (Model/Catalog Number: -) is a medical device manufactured by Research and Production Company «Monitor» Limited. This product is indexed under FDA Product Code / Category Classification Z12150101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
-
Product Code / EMDN
Z12150101
Device Name
Spirometer SMP 21/01 RD
Database Sync Date
2026-08-09 17:59:22

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 Spirometer SMP 21/01 RD?

The registered manufacturer of record for Spirometer SMP 21/01 RD is Research and Production Company «Monitor» Limited.

What is the Primary UDI-DI identifier for Spirometer SMP 21/01 RD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04640003830455.

What classification code is assigned to this device?

This device is registered under product classification code Z12150101.

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