GUDIDData
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gudid Primary ID: RE-21466

RESUSCITATOR MANOMETER POP OFF ADULT (UDI RE-21466)

Manufactured by BESMED HEALTH BUSINESS CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RESUSCITATOR MANOMETER POP OFF ADULT - Primary ID RE-21466

Device Regulatory Overview

The RESUSCITATOR MANOMETER POP OFF ADULT (Model/Catalog Number: RE-21466) is a medical device manufactured by BESMED HEALTH BUSINESS CORP.. This product is indexed under FDA Product Code / Category Classification CAP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RE-21466
Product Code / EMDN
CAP
Device Name
Database Sync Date
2026-08-09 09:15:29

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 RESUSCITATOR MANOMETER POP OFF ADULT?

The registered manufacturer of record for RESUSCITATOR MANOMETER POP OFF ADULT is BESMED HEALTH BUSINESS CORP..

What is the Primary UDI-DI identifier for RESUSCITATOR MANOMETER POP OFF ADULT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RE-21466.

What classification code is assigned to this device?

This device is registered under product classification code CAP.

Similar Classification Devices (CAP)

Other Devices by BESMED HEALTH BUSINESS CORP.

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