SONOCO PLASTICS B.V.

FDA Device Registration & Listing · Berkel en Rodenrijs Zuid-Holland, NL · Registration 3009884346

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
3009884346
FEI Number
3009884346
Entity Name
SONOCO PLASTICS B.V.
City/State/Country
Berkel en Rodenrijs Zuid-Holland, NL
Establishment Address
Veilingweg 24, Berkel en Rodenrijs Zuid-Holland 2651 BE, NL
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Sonoco Plastics b.v. (Owner Number: 10042682)
Owner / Operator Contact Address
Veilingweg 24, Berkel en Rodenrijs, NL-ZH 2651 BE, NL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ventrain

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 2019-06-24

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Sonoco Plastics b.v.
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 3009884346. Last updated year: 2026. Please use registration number 3009884346 when referencing this establishment in official correspondence.
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