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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 3 of 4
DeviceModel / ReferenceRegistriesClassStatus
AmerisourceBergen 10122
FDA UDI
Class IActive
AmerisourceBergen 10542
FDA UDI
Class IIUnknown
Amerisource Bergen 10050
FDA UDI
Class IUnknown
Amerisource Bergen 11305
FDA UDI
Class IActive
AmerisourceBergen 10537
FDA UDI
Class IIUnknown
Amerisource Bergen 11301
FDA UDI
Class IActive
Amerisource Bergen 10906
FDA UDI
Class IActive
AmerisourceBergen 10057
FDA UDI
Class IActive
AmerisourceBergen 10270
FDA UDI
Class IActive
AmerisourceBergen 11501
FDA UDI
Class IActive
AmerisourceBergen 10022
FDA UDI
Class IActive
AmerisourceBergen 10548
FDA UDI
Class IIActive
AmerisourceBergen 11304
FDA UDI
Class IActive
AmerisourceBergen 10031
FDA UDI
Class IUnknown
AmerisourceBergen 10273
FDA UDI
Class IActive
AmerisourceBergen 10042
FDA UDI
Class IActive
AmerisourceBergen 11206
FDA UDI
Class IActive
AmerisourceBergen 10027
FDA UDI
Class IUnknown
Amerisource Bergen 10657
FDA UDI
Class IActive
AmerisourceBergen 10276
FDA UDI
Class IActive
Amerisource Bergen 10130
FDA UDI
Class IActive
Amerisource Bergen 10111
FDA UDI
Class IActive
AmerisourceBergen 10339
FDA UDI
Class IActive
AmerisourceBergen 10039
FDA UDI
Class IActive
Amerisource Bergen 10113
FDA UDI
Class IActive
AmerisourceBergen 10218
FDA UDI
Class IActive
AmerisourceBergen 10332
FDA UDI
Class IActive
Amerisource Bergen 10801
FDA UDI
Class IActive
Amerisource Bergen 10014
FDA UDI
Class IActive
AmerisourceBergen 11404
FDA UDI
Class IActive
AmerisourceBergen 10023
FDA UDI
Class IActive
AmerisourceBergen 10336
FDA UDI
Class IActive
AmerisourceBergen 10037
FDA UDI
Class IActive
Amerisource Bergen 10907
FDA UDI
Class IActive
AmerisourceBergen 10325
FDA UDI
Class IActive
AmerisourceBergen 10255
FDA UDI
Class IActive
AmerisourceBergen 10038
FDA UDI
Class IActive
Amerisource Bergen 10052
FDA UDI
Class IUnknown
AmerisourceBergen 10326
FDA UDI
Class IActive
AmerisourceBergen 10331
FDA UDI
Class IActive
AmerisourceBergen 10055
FDA UDI
Class IActive
AmerisourceBergen DMT-4132
FDA UDI
Class IIActive
Amerisource Bergen 10110
FDA UDI
Class IActive
AmerisourceBergen 10244
FDA UDI
Class IActive
AmerisourceBergen 11502
FDA UDI
Class IActive
AmerisourceBergen 10018
FDA UDI
Class IActive
Amerisource Bergen 10012
FDA UDI
Class IUnknown
Amerisource Bergen 10117
FDA UDI
Class IActive
AmerisourceBergen 10119
FDA UDI
Class IActive
Amerisource Bergen 10660
FDA UDI
Class IActive

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