TMR PLASTICS

FDA Device Registration & Listing · Bydgoszcz Pomorskie, PL · Registration 3030433705

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
3030433705
FEI Number
3030433705
Entity Name
TMR PLASTICS
City/State/Country
Bydgoszcz Pomorskie, PL
Establishment Address
ul. Bydgoskich Przemyslowcow 5, Bydgoszcz Pomorskie PL 85-862, PL
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TMR Plastics (Owner Number: 10090551)
Owner / Operator Contact Address
ul. Bydgoskich Przemyslowcow 5, Bydgoszcz, PL-NOTA PL 85-862, PL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bedal INTRAVASCULAR CATHETER SECUREMENT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2024-04-11

Official Correspondent

Blazej Lojewski

US Agent Details

Cherita James Business: Pro Pharma Group Email: cherita.james@propharmagroup.com Phone: (347) 9540624

Related Public Records

Same Entity

TMR Plastics
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030433705. Last updated year: 2026. Please use registration number 3030433705 when referencing this establishment in official correspondence.
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