gudid Primary ID: 36-SM2125

Calibration Pump (UDI 36-SM2125)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Calibration Pump (Model/Catalog Number: 36-SM2125) is a medical device manufactured by Jaeger Medical GmbH. This product is indexed under FDA Product Code / Category Classification BXW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 36-SM2125
Product Code / EMDN: BXW
Device Name: Calibration Pump 3 Liter
Database Sync Date: 2026-08-09 09:59:20

Full Regulatory Attributes

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{
    "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 Calibration Pump?

The registered manufacturer of record for Calibration Pump is Jaeger Medical GmbH.

What is the Primary UDI-DI identifier for Calibration Pump?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 36-SM2125.

What classification code is assigned to this device?

This device is registered under product classification code BXW.

Similar Classification Devices (BXW)

Other Devices by Jaeger Medical GmbH

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