TAMABIO CO.,LTD.

FDA Device Registration & Listing · Musashino-shi Tokyo, JP · Registration 3041851334

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
3041851334
FEI Number
3041851334
Entity Name
TAMABIO CO.,LTD.
City/State/Country
Musashino-shi Tokyo, JP
Establishment Address
402 2-2-18 Sakai, Musashino-shi Tokyo 180-0022, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TamaBio Co.,Ltd. (Owner Number: 10094178)
Owner / Operator Contact Address
402 2-2-18 Sakai, Musashino-shi, JP-13 180-0022, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

PeriBeam

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene Cardiovascular Class 2 870.3470 2025-11-18

Official Correspondent

Tetsuya Nagao

US Agent Details

Keiji Asada Business: Amenichi Consulting, LLC. Email: keiji.asada@amenichi.com Phone: (312) 9332887

Related Public Records

Same Entity

TamaBio Co.,Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3041851334. Last updated year: 2026. Please use registration number 3041851334 when referencing this establishment in official correspondence.
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