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PISA BIOPHARM INC.

US

Last updated May 27, 2026

What PISA BIOPHARM INC. makes

PiSA Biopharm Inc. manufactures intravenous administration bags designed for the delivery of pharmaceutical solutions, including sterile fluids and medications. These products are intended for hospital and clinical use to ensure controlled infusion of treatments.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

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 PiSA Biopharm Inc. manufacture?

PiSA Biopharm Inc. specializes in intravenous administration bags, which are used to deliver sterile fluids and medications in controlled infusions. These devices are primarily designed for hospital and clinical settings to ensure precise and safe administration of pharmaceutical treatments.

Where is PiSA Biopharm Inc. based?

PiSA Biopharm Inc. is headquartered in the United States. The company’s location supports its focus on manufacturing and distributing intravenous administration devices tailored for healthcare environments.

How are PiSA Biopharm Inc.’s devices classified under FDA regulations?

PiSA Biopharm Inc.’s intravenous administration bags fall under Class II medical device classification according to FDA guidelines. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness.

Are PiSA Biopharm Inc.’s devices listed in any regulatory databases?

Yes, PiSA Biopharm Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This listing helps ensure traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to identify and verify the devices.

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

Information

Country
US
Address
—
LinkedIn
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Facebook
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Phone
5189925044
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
080043343

Catalogue (20)

DeviceModel / ReferenceRegistriesClassStatus
PiSA BioPharm 600206
FDA UDI
Class IIActive
PiSA BioPharm 60010
FDA UDI
Class IIActive
PiSA BioPharm 600202
FDA UDI
Class IIActive
PiSA BioPharm 600203
FDA UDI
Class IIActive
PiSA BioPharm 60012
FDA UDI
Class IIActive
PiSA BioPharm 60004
FDA UDI
Class IIActive
PiSA BioPharm 60009
FDA UDI
Class IIActive
PiSA BioPharm 600201
FDA UDI
Class IIActive
PiSA BioPharm 60003
FDA UDI
Class IIActive
PiSA BioPharm 60011
FDA UDI
Class IIActive
PiSA BioPharm 60014
FDA UDI
Class IIActive
PiSA BioPharm 60005
FDA UDI
Class IIActive
PiSA BioPharm 60006
FDA UDI
Class IIActive
PiSA BioPharm 600204
FDA UDI
Class IIActive
PiSA BioPharm 60008
FDA UDI
Class IIActive
PiSA BioPharm 60007
FDA UDI
Class IIActive
PiSA BioPharm 60001
FDA UDI
Class IIActive
PiSA BioPharm 60013
FDA UDI
Class IIActive
PiSA BioPharm 60002
FDA UDI
Class IIActive
PiSA BioPharm 600205
FDA UDI
Class IIActive

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