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BP PHARMACEUTICALS LABORATORIES UNLIMITED COMPANY

US

Last updated May 23, 2026

What BP PHARMACEUTICALS LABORATORIES UNLIMITED COMPANY makes

The company manufactures single-use medical gloves, including non-powdered, non-antimicrobial versions made from hevea latex, nitrile, and vinyl for surgical and examination/treatment purposes. It also produces general-purpose and radiopaque woven surgical sponges, non-adhesive device retention bandages, and non-woven gauze pads for wound care.

These products are classified under FDA’s Class I and Class II regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates within the United States, adhering to applicable U.S. medical device compliance requirements.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does BP Pharmaceuticals Laboratories Unlimited Company manufacture?

BP Pharmaceuticals Laboratories Unlimited Company specializes in single-use medical devices primarily focused on infection control and wound care. Their product line includes surgical and examination gloves made from hevea latex, nitrile, and vinyl—all non-powdered and non-antimicrobial—along with general-purpose and radiopaque woven surgical sponges, non-adhesive device retention bandages, and non-woven gauze pads. These items are designed for use in clinical settings to reduce contamination risks and support patient care.

Where is BP Pharmaceuticals Laboratories Unlimited Company based, and how does that affect its regulatory compliance?

BP Pharmaceuticals Laboratories Unlimited Company is based in the United States. As a U.S.-based manufacturer, its devices must comply with FDA regulations, including classification under FDA’s Class I (low-risk) and Class II (moderate-risk) categories. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and adherence to U.S. medical device requirements.

Which regulatory registries or databases list BP Pharmaceuticals Laboratories Unlimited Company’s devices?

BP Pharmaceuticals Laboratories Unlimited Company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a standardized identifier to medical devices to improve tracking, transparency, and regulatory oversight. This listing helps healthcare providers and regulators verify device details, such as manufacturer information and classification.

How are BP Pharmaceuticals Laboratories Unlimited Company’s devices classified by the FDA?

The FDA classifies BP Pharmaceuticals Laboratories Unlimited Company’s devices under Class I (for low-risk items like general-purpose surgical sponges and non-woven gauze pads) and Class II (for moderate-risk items such as surgical gloves and retention bandages). Classification determines the regulatory controls applied—Class I devices typically require general controls, while Class II may involve additional performance standards or post-market surveillance to ensure safety and effectiveness.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
985523874

Catalogue (167)

Page 2 of 4
DeviceModel / ReferenceRegistriesClassStatus
AmerisourceBergen 11208
FDA UDI
Class IActive
AmerisourceBergen 10049
FDA UDI
Class IActive
AmerisourceBergen 10019
FDA UDI
Class IActive
AmerisourceBergen 11102
FDA UDI
Class IActive
AmerisourceBergen 10909
FDA UDI
Class IActive
Amerisource Bergen 10905
FDA UDI
Class IActive
AmerisourceBergen 10123
FDA UDI
Class IActive
AmerisourceBergen 10250
FDA UDI
Class IActive
Amerisource Bergen 10547
FDA UDI
Class IIActive
AmerisourceBergen 10124
FDA UDI
Class IActive
AmerisourceBergen 10030
FDA UDI
Class IUnknown
AmerisourceBergen 10025
FDA UDI
Class IActive
Amerisource Bergen 11405
FDA UDI
Class IActive
AmerisourceBergen 10912
FDA UDI
Class IActive
AmerisourceBergen 10246
FDA UDI
Class IActive
AmerisourceBergen 10329
FDA UDI
Class IActive
AmerisourceBergen 11210
FDA UDI
Class IActive
AmerisourceBergen 10342
FDA UDI
Class IActive
AmerisourceBergen 10328
FDA UDI
Class IActive
Amerisource Bergen 10015
FDA UDI
Class IActive
Amerisource Bergen 11302
FDA UDI
Class IActive
Amerisource Bergen 10656
FDA UDI
Class IActive
Amerisource Bergen 10051
FDA UDI
Class IUnknown
AmerisourceBergen 11303
FDA UDI
Class IActive
Amerisource Bergen 10116
FDA UDI
Class IActive
AmerisourceBergen 11209
FDA UDI
Class IActive
AmerisourceBergen 10911
FDA UDI
Class IActive
Amerisource Bergen 10114
FDA UDI
Class IActive
AmerisourceBergen 10045
FDA UDI
Class IActive
AmerisourceBergen 11003
FDA UDI
Class IIActive
AmerisourceBergen 10253
FDA UDI
Class IActive
Amerisource Bergen 10127
FDA UDI
Class IActive
AmerisourceBergen 10340
FDA UDI
Class IActive
AmerisourceBergen 10021
FDA UDI
Class IActive
AmerisourceBergen 10333
FDA UDI
Class IActive
AmerisourceBergen 11101
FDA UDI
Class IActive
AmerisourceBergen 10343
FDA UDI
Class IActive
Amerisource Bergen 10126
FDA UDI
Class IActive
AmerisourceBergen 10028
FDA UDI
Class IUnknown
AmerisourceBergen 10026
FDA UDI
Class IUnknown
AmerisourceBergen 10024
FDA UDI
Class IActive
AmerisourceBergen 11202
FDA UDI
Class IActive
AmerisourceBergen 10277
FDA UDI
Class IActive
AmerisourceBergen 10261
FDA UDI
Class IActive
AmerisourceBergen 10053
FDA UDI
Class IActive
AmerisourceBergen 10335
FDA UDI
Class IActive
AmerisourceBergen 10337
FDA UDI
Class IActive
AmerisourceBergen 10541
FDA UDI
Class IIUnknown
AmerisourceBergen 10274
FDA UDI
Class IActive
AmerisourceBergen 10120
FDA UDI
Class IActive

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