Bio-Med Healthcare Products Pvt. Ltd.

FDA Device Registration & Listing · Palwal Haryana, IN · Registration 3015314035

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
3015314035
FEI Number
3015314035
Entity Name
Bio-Med Healthcare Products Pvt. Ltd.
City/State/Country
Palwal Haryana, IN
Establishment Address
49/4 Main Mathura Road, Prithla, Palwal Haryana 121102, IN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
BIO-MED HEALTHCARE PRODUCTS PVT (Owner Number: 10095571)
Owner / Operator Contact Address
49/4, Mathura Road, Prithla, Palwal, IN-HR 121102, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Capnoflow

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2026-04-01

Official Correspondent

Deepak Arora

US Agent Details

John Brown Business: Arete Medical Devices Email: john@aretemedicaldevices.com Phone: (267) 3742587

Related Public Records

Same Entity

BIO-MED HEALTHCARE PRODUCTS PVT
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2014 King Systems Corp. 1
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015314035. Last updated year: 2026. Please use registration number 3015314035 when referencing this establishment in official correspondence.
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