INTERNATIONAL EMERGENCY SERVICES S.L

FDA Device Registration & Listing · Derio Bizkaia Vizcaya, ES · Registration 3031754300

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3031754300
FEI Number
3031754300
Entity Name
INTERNATIONAL EMERGENCY SERVICES S.L
City/State/Country
Derio Bizkaia Vizcaya, ES
Establishment Address
Bizkaia Science and Technology Park, Ibaizabal bidea, 500, Derio Bizkaia Vizcaya E-48160, ES
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
International Emergency Services S.L (Owner Number: 10091148)
Owner / Operator Contact Address
Bizkaia Science and Technology Park, Ibaizabal bidea, 500, Derio Bizkaia, ES-BI E-48160, ES
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Tritube Ventrain Cricath Evone Ventinova

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BTL Ventilator, Emergency, Powered (Resuscitator) Anesthesiology Class 2 868.5925 2024-07-12

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

International Emergency Services S.L
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K862192 U.O. Equipment Co. RESUSCITATOR MODELS 10400/10500/10600/10700/10800 1986-07-07

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0004-2025 Mercury Enterprises, Inc. dba Mercury Medical 2
Neo-Tee T-Piece Resuscitator. Part Numbers 1050805, 1050832. For pediatric emergency respiratory support.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031754300. Last updated year: 2026. Please use registration number 3031754300 when referencing this establishment in official correspondence.
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