MYLAN PHARMACEUTICALS INC.

FDA Device Registration & Listing · Morgantown, WV, US · Registration 1110315

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
1110315
FEI Number
1110315
Entity Name
MYLAN PHARMACEUTICALS INC.
City/State/Country
Morgantown, WV, US
Establishment Address
3711 Collins Ferry Road, Morgantown, WV 26505, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Mylan Pharmaceuticals Inc. (Owner Number: 10047905)
Owner / Operator Contact Address
3711 Collins Ferry Road, Morgantown, WV 26505, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Whisperject Sodium Chloride 3% and 10%

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZH Introducer, Syringe Needle General Hospital Class 2 880.6920 2017-12-06
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2017-01-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mylan Pharmaceuticals Inc.
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
K163485 Adherium (Nz), Ltd. SmartTouch 2017-08-30
K781467 Travenol Laboratories, S.A. U-FLOAT VALVE 2D9023 1978-09-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1110315. Last updated year: 2026. Please use registration number 1110315 when referencing this establishment in official correspondence.
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